Canonical Allele Identifier: CA377159795

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73560396G>T (hg19) ; chr10:g.71800639G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71800639G>T , CM000672.2:g.71800639G>T	GRCh38
NC_000010.10:g.73560396G>T , CM000672.1:g.73560396G>T	GRCh37
NC_000010.9:g.73230402G>T	NCBI36
NG_008835.1:g.408693G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7366G>T MANE Select	ENSP00000224721.9:p.Asp2456Tyr
ENST00000642965.1:c.1299G>T	ENSP00000495222.1:n.1299G>T
ENST00000647092.1:c.963G>T	ENSP00000495176.1:n.963G>T
ENST00000224721.10:c.7381G>T	ENSP00000224721.8:p.Asp2461Tyr
ENST00000398788.4:c.646G>T	ENSP00000381768.3:p.Asp216Tyr
ENST00000475158.1:n.902G>T
ENST00000619887.4:c.646G>T	ENSP00000478374.1:p.Asp216Tyr
ENST00000622827.4:c.7366G>T	ENSP00000483211.1:p.Asp2456Tyr
NM_001171933.1:c.646G>T	NP_001165404.1:p.Asp216Tyr
NM_001171934.1:c.646G>T	NP_001165405.1:p.Asp216Tyr
NM_022124.5:c.7366G>T	NP_071407.4:p.Asp2456Tyr
XM_006717940.2:c.7561G>T	XP_006718003.1:p.Asp2521Tyr
XM_006717942.2:c.7495G>T	XP_006718005.1:p.Asp2499Tyr
XM_011540039.1:c.7558G>T	XP_011538341.1:p.Asp2520Tyr
XM_011540040.1:c.7555G>T	XP_011538342.1:p.Asp2519Tyr
XM_011540041.1:c.7501G>T	XP_011538343.1:p.Asp2501Tyr
XM_011540042.1:c.7471G>T	XP_011538344.1:p.Asp2491Tyr
XM_011540043.1:c.7561G>T	XP_011538345.1:p.Asp2521Tyr
XM_011540044.1:c.7426G>T	XP_011538346.1:p.Asp2476Tyr
XM_011540045.1:c.7561G>T	XP_011538347.1:p.Asp2521Tyr
XM_011540046.1:c.7021G>T	XP_011538348.1:p.Asp2341Tyr
XM_011540047.1:c.6379G>T	XP_011538349.1:p.Asp2127Tyr
XM_011540052.1:c.3889G>T	XP_011538354.1:p.Asp1297Tyr
NM_022124.6:c.7366G>T MANE Select	NP_071407.4:p.Asp2456Tyr