Canonical Allele Identifier: CA377159418

Gene: CDH23

Linked Data

• COSMIC: COSM3981113
• MyVariant Identifiers: chr10:g.73559323C>A (hg19) ; chr10:g.71799566C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799566C>A , CM000672.2:g.71799566C>A	GRCh38
NC_000010.10:g.73559323C>A , CM000672.1:g.73559323C>A	GRCh37
NC_000010.9:g.73229329C>A	NCBI36
NG_008835.1:g.407620C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7299C>A MANE Select	ENSP00000224721.9:p.Asn2433Lys
ENST00000642965.1:c.1232C>A	ENSP00000495222.1:n.1232C>A
ENST00000647092.1:c.896C>A	ENSP00000495176.1:n.896C>A
ENST00000224721.10:c.7314C>A	ENSP00000224721.8:p.Asn2438Lys
ENST00000398788.4:c.579C>A	ENSP00000381768.3:p.Asn193Lys
ENST00000475158.1:n.835C>A
ENST00000619887.4:c.579C>A	ENSP00000478374.1:p.Asn193Lys
ENST00000622827.4:c.7299C>A	ENSP00000483211.1:p.Asn2433Lys
NM_001171933.1:c.579C>A	NP_001165404.1:p.Asn193Lys
NM_001171934.1:c.579C>A	NP_001165405.1:p.Asn193Lys
NM_022124.5:c.7299C>A	NP_071407.4:p.Asn2433Lys
XM_006717940.2:c.7494C>A	XP_006718003.1:p.Asn2498Lys
XM_006717942.2:c.7428C>A	XP_006718005.1:p.Asn2476Lys
XM_011540039.1:c.7491C>A	XP_011538341.1:p.Asn2497Lys
XM_011540040.1:c.7488C>A	XP_011538342.1:p.Asn2496Lys
XM_011540041.1:c.7434C>A	XP_011538343.1:p.Asn2478Lys
XM_011540042.1:c.7404C>A	XP_011538344.1:p.Asn2468Lys
XM_011540043.1:c.7494C>A	XP_011538345.1:p.Asn2498Lys
XM_011540044.1:c.7359C>A	XP_011538346.1:p.Asn2453Lys
XM_011540045.1:c.7494C>A	XP_011538347.1:p.Asn2498Lys
XM_011540046.1:c.6954C>A	XP_011538348.1:p.Asn2318Lys
XM_011540047.1:c.6312C>A	XP_011538349.1:p.Asn2104Lys
XM_011540052.1:c.3822C>A	XP_011538354.1:p.Asn1274Lys
NM_022124.6:c.7299C>A MANE Select	NP_071407.4:p.Asn2433Lys