Canonical Allele Identifier: CA1918884961

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71806193G= , CM000672.2:g.71806193G=	GRCh38
NC_000010.10:g.73565950G= , CM000672.1:g.73565950G=	GRCh37
NC_000010.9:g.73235956G=	NCBI36
NG_008835.1:g.414247G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8090G= MANE Select	ENSP00000224721.9:p.Gly2697=
ENST00000642965.1:c.2023G=	ENSP00000495222.1:n.2023G=
ENST00000647092.1:c.1687G=	ENSP00000495176.1:n.1687G=
ENST00000224721.10:c.8105G=	ENSP00000224721.8:p.Gly2702=
ENST00000398788.4:c.1370G=	ENSP00000381768.3:p.Gly457=
ENST00000475158.1:n.1626G=
ENST00000619887.4:c.1370G=	ENSP00000478374.1:p.Gly457=
ENST00000622827.4:c.8090G=	ENSP00000483211.1:p.Gly2697=
NM_001171933.1:c.1370G=	NP_001165404.1:p.Gly457=
NM_001171934.1:c.1370G=	NP_001165405.1:p.Gly457=
NM_022124.5:c.8090G=	NP_071407.4:p.Gly2697=
XM_006717940.2:c.8285G=	XP_006718003.1:p.Gly2762=
XM_006717942.2:c.8219G=	XP_006718005.1:p.Gly2740=
XM_011540039.1:c.8282G=	XP_011538341.1:p.Gly2761=
XM_011540040.1:c.8279G=	XP_011538342.1:p.Gly2760=
XM_011540041.1:c.8225G=	XP_011538343.1:p.Gly2742=
XM_011540042.1:c.8195G=	XP_011538344.1:p.Gly2732=
XM_011540043.1:c.8285G=	XP_011538345.1:p.Gly2762=
XM_011540044.1:c.8150G=	XP_011538346.1:p.Gly2717=
XM_011540045.1:c.8285G=	XP_011538347.1:p.Gly2762=
XM_011540046.1:c.7745G=	XP_011538348.1:p.Gly2582=
XM_011540047.1:c.7103G=	XP_011538349.1:p.Gly2368=
XM_011540052.1:c.4613G=	XP_011538354.1:p.Gly1538=
NM_022124.6:c.8090G= MANE Select	NP_071407.4:p.Gly2697=