Canonical Allele Identifier: CA1918880451

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71803053C= , CM000672.2:g.71803053C=	GRCh38
NC_000010.10:g.73562810C= , CM000672.1:g.73562810C=	GRCh37
NC_000010.9:g.73232816C=	NCBI36
NG_008835.1:g.411107C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7638C= MANE Select	ENSP00000224721.9:p.Tyr2546=
ENST00000642965.1:c.1571C=	ENSP00000495222.1:n.1571C=
ENST00000647092.1:c.1235C=	ENSP00000495176.1:n.1235C=
ENST00000224721.10:c.7653C=	ENSP00000224721.8:p.Tyr2551=
ENST00000398788.4:c.918C=	ENSP00000381768.3:p.Tyr306=
ENST00000475158.1:n.1174C=
ENST00000619887.4:c.918C=	ENSP00000478374.1:p.Tyr306=
ENST00000622827.4:c.7638C=	ENSP00000483211.1:p.Tyr2546=
NM_001171933.1:c.918C=	NP_001165404.1:p.Tyr306=
NM_001171934.1:c.918C=	NP_001165405.1:p.Tyr306=
NM_022124.5:c.7638C=	NP_071407.4:p.Tyr2546=
XM_006717940.2:c.7833C=	XP_006718003.1:p.Tyr2611=
XM_006717942.2:c.7767C=	XP_006718005.1:p.Tyr2589=
XM_011540039.1:c.7830C=	XP_011538341.1:p.Tyr2610=
XM_011540040.1:c.7827C=	XP_011538342.1:p.Tyr2609=
XM_011540041.1:c.7773C=	XP_011538343.1:p.Tyr2591=
XM_011540042.1:c.7743C=	XP_011538344.1:p.Tyr2581=
XM_011540043.1:c.7833C=	XP_011538345.1:p.Tyr2611=
XM_011540044.1:c.7698C=	XP_011538346.1:p.Tyr2566=
XM_011540045.1:c.7833C=	XP_011538347.1:p.Tyr2611=
XM_011540046.1:c.7293C=	XP_011538348.1:p.Tyr2431=
XM_011540047.1:c.6651C=	XP_011538349.1:p.Tyr2217=
XM_011540052.1:c.4161C=	XP_011538354.1:p.Tyr1387=
NM_022124.6:c.7638C= MANE Select	NP_071407.4:p.Tyr2546=