Hs06961680_cn

• Gene Symbol: ANKRD13A
• Assay Reference Genome Location: Chr.12:110010279 on build GRCh38
• Cytoband: 12q24.11

Target Gene Details

• Entrez Gene ID: 88455
• Gene Name: ankyrin repeat domain 13A
• Gene Aliases: ANKRD13, NY-REN-25
• Location: Chr.12:109999169-110039432 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ANKRD13A	NM_033121.1			NP_149112.1
	XM_005253980.2			XP_005254037.1
	XM_005253981.3			XP_005254038.1
	XM_005253982.3			XP_005254039.1
	XM_005253984.1			XP_005254041.1
	XM_011538937.1			XP_011537239.1
	XM_011538938.2			XP_011537240.1
	XM_017020157.1			XP_016875646.1
	XM_017020158.1			XP_016875647.1
	XM_017020159.1			XP_016875648.1
	XM_017020160.1			XP_016875649.1
	XM_017020161.1			XP_016875650.1
	XM_017020162.1			XP_016875651.1
	XM_017020163.1			XP_016875652.1
	AF064604.1			AAC17109.1
	AK025261.1
	AK302535.1
	AK308923.1
	AY364251.1			AAQ76810.1
	BC032833.2			AAH32833.2

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv884	Chr.12:109977151 - 110010582 on Build GRCh38	Insertion	ANKRD13A GIT2

More Information

Additional Information:

For this assay, SNP(s) [rs73205046] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

• Set Membership: Intragenic, Intronic, Non-exonic, DGV Variation