Canonical Allele Identifier: CA377159845

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73560414T>A (hg19) ; chr10:g.71800657T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71800657T>A , CM000672.2:g.71800657T>A	GRCh38
NC_000010.10:g.73560414T>A , CM000672.1:g.73560414T>A	GRCh37
NC_000010.9:g.73230420T>A	NCBI36
NG_008835.1:g.408711T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7384T>A MANE Select	ENSP00000224721.9:p.Ser2462Thr
ENST00000642965.1:c.1317T>A	ENSP00000495222.1:n.1317T>A
ENST00000647092.1:c.981T>A	ENSP00000495176.1:n.981T>A
ENST00000224721.10:c.7399T>A	ENSP00000224721.8:p.Ser2467Thr
ENST00000398788.4:c.664T>A	ENSP00000381768.3:p.Ser222Thr
ENST00000475158.1:n.920T>A
ENST00000619887.4:c.664T>A	ENSP00000478374.1:p.Ser222Thr
ENST00000622827.4:c.7384T>A	ENSP00000483211.1:p.Ser2462Thr
NM_001171933.1:c.664T>A	NP_001165404.1:p.Ser222Thr
NM_001171934.1:c.664T>A	NP_001165405.1:p.Ser222Thr
NM_022124.5:c.7384T>A	NP_071407.4:p.Ser2462Thr
XM_006717940.2:c.7579T>A	XP_006718003.1:p.Ser2527Thr
XM_006717942.2:c.7513T>A	XP_006718005.1:p.Ser2505Thr
XM_011540039.1:c.7576T>A	XP_011538341.1:p.Ser2526Thr
XM_011540040.1:c.7573T>A	XP_011538342.1:p.Ser2525Thr
XM_011540041.1:c.7519T>A	XP_011538343.1:p.Ser2507Thr
XM_011540042.1:c.7489T>A	XP_011538344.1:p.Ser2497Thr
XM_011540043.1:c.7579T>A	XP_011538345.1:p.Ser2527Thr
XM_011540044.1:c.7444T>A	XP_011538346.1:p.Ser2482Thr
XM_011540045.1:c.7579T>A	XP_011538347.1:p.Ser2527Thr
XM_011540046.1:c.7039T>A	XP_011538348.1:p.Ser2347Thr
XM_011540047.1:c.6397T>A	XP_011538349.1:p.Ser2133Thr
XM_011540052.1:c.3907T>A	XP_011538354.1:p.Ser1303Thr
NM_022124.6:c.7384T>A MANE Select	NP_071407.4:p.Ser2462Thr