Canonical Allele Identifier: CA1918878477

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798511G= , CM000672.2:g.71798511G=	GRCh38
NC_000010.10:g.73558268G= , CM000672.1:g.73558268G=	GRCh37
NC_000010.9:g.73228274G=	NCBI36
NG_008835.1:g.406565G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6987G= MANE Select	ENSP00000224721.9:p.Gly2329=
ENST00000642965.1:c.920G=	ENSP00000495222.1:n.920G=
ENST00000647092.1:c.584G=	ENSP00000495176.1:n.584G=
ENST00000224721.10:c.7002G=	ENSP00000224721.8:p.Gly2334=
ENST00000398788.4:c.267G=	ENSP00000381768.3:p.Gly89=
ENST00000475158.1:n.523G=
ENST00000619887.4:c.267G=	ENSP00000478374.1:p.Gly89=
ENST00000622827.4:c.6987G=	ENSP00000483211.1:p.Gly2329=
NM_001171933.1:c.267G=	NP_001165404.1:p.Gly89=
NM_001171934.1:c.267G=	NP_001165405.1:p.Gly89=
NM_022124.5:c.6987G=	NP_071407.4:p.Gly2329=
XM_006717940.2:c.7182G=	XP_006718003.1:p.Gly2394=
XM_006717942.2:c.7116G=	XP_006718005.1:p.Gly2372=
XM_011540039.1:c.7179G=	XP_011538341.1:p.Gly2393=
XM_011540040.1:c.7176G=	XP_011538342.1:p.Gly2392=
XM_011540041.1:c.7122G=	XP_011538343.1:p.Gly2374=
XM_011540042.1:c.7092G=	XP_011538344.1:p.Gly2364=
XM_011540043.1:c.7182G=	XP_011538345.1:p.Gly2394=
XM_011540044.1:c.7047G=	XP_011538346.1:p.Gly2349=
XM_011540045.1:c.7182G=	XP_011538347.1:p.Gly2394=
XM_011540046.1:c.6642G=	XP_011538348.1:p.Gly2214=
XM_011540047.1:c.6000G=	XP_011538349.1:p.Gly2000=
XM_011540052.1:c.3510G=	XP_011538354.1:p.Gly1170=
NM_022124.6:c.6987G= MANE Select	NP_071407.4:p.Gly2329=