Canonical Allele Identifier: CA1918878498

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798548G= , CM000672.2:g.71798548G=	GRCh38
NC_000010.10:g.73558305G= , CM000672.1:g.73558305G=	GRCh37
NC_000010.9:g.73228311G=	NCBI36
NG_008835.1:g.406602G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7024G= MANE Select	ENSP00000224721.9:p.Gly2342=
ENST00000642965.1:c.957G=	ENSP00000495222.1:n.957G=
ENST00000647092.1:c.621G=	ENSP00000495176.1:n.621G=
ENST00000224721.10:c.7039G=	ENSP00000224721.8:p.Gly2347=
ENST00000398788.4:c.304G=	ENSP00000381768.3:p.Gly102=
ENST00000475158.1:n.560G=
ENST00000619887.4:c.304G=	ENSP00000478374.1:p.Gly102=
ENST00000622827.4:c.7024G=	ENSP00000483211.1:p.Gly2342=
NM_001171933.1:c.304G=	NP_001165404.1:p.Gly102=
NM_001171934.1:c.304G=	NP_001165405.1:p.Gly102=
NM_022124.5:c.7024G=	NP_071407.4:p.Gly2342=
XM_006717940.2:c.7219G=	XP_006718003.1:p.Gly2407=
XM_006717942.2:c.7153G=	XP_006718005.1:p.Gly2385=
XM_011540039.1:c.7216G=	XP_011538341.1:p.Gly2406=
XM_011540040.1:c.7213G=	XP_011538342.1:p.Gly2405=
XM_011540041.1:c.7159G=	XP_011538343.1:p.Gly2387=
XM_011540042.1:c.7129G=	XP_011538344.1:p.Gly2377=
XM_011540043.1:c.7219G=	XP_011538345.1:p.Gly2407=
XM_011540044.1:c.7084G=	XP_011538346.1:p.Gly2362=
XM_011540045.1:c.7219G=	XP_011538347.1:p.Gly2407=
XM_011540046.1:c.6679G=	XP_011538348.1:p.Gly2227=
XM_011540047.1:c.6037G=	XP_011538349.1:p.Gly2013=
XM_011540052.1:c.3547G=	XP_011538354.1:p.Gly1183=
NM_022124.6:c.7024G= MANE Select	NP_071407.4:p.Gly2342=