Canonical Allele Identifier: CA1918878472

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798501G= , CM000672.2:g.71798501G=	GRCh38
NC_000010.10:g.73558258G= , CM000672.1:g.73558258G=	GRCh37
NC_000010.9:g.73228264G=	NCBI36
NG_008835.1:g.406555G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6977G= MANE Select	ENSP00000224721.9:p.Gly2326=
ENST00000642965.1:c.910G=	ENSP00000495222.1:n.910G=
ENST00000647092.1:c.574G=	ENSP00000495176.1:n.574G=
ENST00000224721.10:c.6992G=	ENSP00000224721.8:p.Gly2331=
ENST00000398788.4:c.257G=	ENSP00000381768.3:p.Gly86=
ENST00000475158.1:n.513G=
ENST00000619887.4:c.257G=	ENSP00000478374.1:p.Gly86=
ENST00000622827.4:c.6977G=	ENSP00000483211.1:p.Gly2326=
NM_001171933.1:c.257G=	NP_001165404.1:p.Gly86=
NM_001171934.1:c.257G=	NP_001165405.1:p.Gly86=
NM_022124.5:c.6977G=	NP_071407.4:p.Gly2326=
XM_006717940.2:c.7172G=	XP_006718003.1:p.Gly2391=
XM_006717942.2:c.7106G=	XP_006718005.1:p.Gly2369=
XM_011540039.1:c.7169G=	XP_011538341.1:p.Gly2390=
XM_011540040.1:c.7166G=	XP_011538342.1:p.Gly2389=
XM_011540041.1:c.7112G=	XP_011538343.1:p.Gly2371=
XM_011540042.1:c.7082G=	XP_011538344.1:p.Gly2361=
XM_011540043.1:c.7172G=	XP_011538345.1:p.Gly2391=
XM_011540044.1:c.7037G=	XP_011538346.1:p.Gly2346=
XM_011540045.1:c.7172G=	XP_011538347.1:p.Gly2391=
XM_011540046.1:c.6632G=	XP_011538348.1:p.Gly2211=
XM_011540047.1:c.5990G=	XP_011538349.1:p.Gly1997=
XM_011540052.1:c.3500G=	XP_011538354.1:p.Gly1167=
NM_022124.6:c.6977G= MANE Select	NP_071407.4:p.Gly2326=