Canonical Allele Identifier: CA1918879387

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71800649T= , CM000672.2:g.71800649T=	GRCh38
NC_000010.10:g.73560406T= , CM000672.1:g.73560406T=	GRCh37
NC_000010.9:g.73230412T=	NCBI36
NG_008835.1:g.408703T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7376T= MANE Select	ENSP00000224721.9:p.Val2459=
ENST00000642965.1:c.1309T=	ENSP00000495222.1:n.1309T=
ENST00000647092.1:c.973T=	ENSP00000495176.1:n.973T=
ENST00000224721.10:c.7391T=	ENSP00000224721.8:p.Val2464=
ENST00000398788.4:c.656T=	ENSP00000381768.3:p.Val219=
ENST00000475158.1:n.912T=
ENST00000619887.4:c.656T=	ENSP00000478374.1:p.Val219=
ENST00000622827.4:c.7376T=	ENSP00000483211.1:p.Val2459=
NM_001171933.1:c.656T=	NP_001165404.1:p.Val219=
NM_001171934.1:c.656T=	NP_001165405.1:p.Val219=
NM_022124.5:c.7376T=	NP_071407.4:p.Val2459=
XM_006717940.2:c.7571T=	XP_006718003.1:p.Val2524=
XM_006717942.2:c.7505T=	XP_006718005.1:p.Val2502=
XM_011540039.1:c.7568T=	XP_011538341.1:p.Val2523=
XM_011540040.1:c.7565T=	XP_011538342.1:p.Val2522=
XM_011540041.1:c.7511T=	XP_011538343.1:p.Val2504=
XM_011540042.1:c.7481T=	XP_011538344.1:p.Val2494=
XM_011540043.1:c.7571T=	XP_011538345.1:p.Val2524=
XM_011540044.1:c.7436T=	XP_011538346.1:p.Val2479=
XM_011540045.1:c.7571T=	XP_011538347.1:p.Val2524=
XM_011540046.1:c.7031T=	XP_011538348.1:p.Val2344=
XM_011540047.1:c.6389T=	XP_011538349.1:p.Val2130=
XM_011540052.1:c.3899T=	XP_011538354.1:p.Val1300=
NM_022124.6:c.7376T= MANE Select	NP_071407.4:p.Val2459=