Canonical Allele Identifier: CA1918878491

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798533G= , CM000672.2:g.71798533G=	GRCh38
NC_000010.10:g.73558290G= , CM000672.1:g.73558290G=	GRCh37
NC_000010.9:g.73228296G=	NCBI36
NG_008835.1:g.406587G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7009G= MANE Select	ENSP00000224721.9:p.Asp2337=
ENST00000642965.1:c.942G=	ENSP00000495222.1:n.942G=
ENST00000647092.1:c.606G=	ENSP00000495176.1:n.606G=
ENST00000224721.10:c.7024G=	ENSP00000224721.8:p.Asp2342=
ENST00000398788.4:c.289G=	ENSP00000381768.3:p.Asp97=
ENST00000475158.1:n.545G=
ENST00000619887.4:c.289G=	ENSP00000478374.1:p.Asp97=
ENST00000622827.4:c.7009G=	ENSP00000483211.1:p.Asp2337=
NM_001171933.1:c.289G=	NP_001165404.1:p.Asp97=
NM_001171934.1:c.289G=	NP_001165405.1:p.Asp97=
NM_022124.5:c.7009G=	NP_071407.4:p.Asp2337=
XM_006717940.2:c.7204G=	XP_006718003.1:p.Asp2402=
XM_006717942.2:c.7138G=	XP_006718005.1:p.Asp2380=
XM_011540039.1:c.7201G=	XP_011538341.1:p.Asp2401=
XM_011540040.1:c.7198G=	XP_011538342.1:p.Asp2400=
XM_011540041.1:c.7144G=	XP_011538343.1:p.Asp2382=
XM_011540042.1:c.7114G=	XP_011538344.1:p.Asp2372=
XM_011540043.1:c.7204G=	XP_011538345.1:p.Asp2402=
XM_011540044.1:c.7069G=	XP_011538346.1:p.Asp2357=
XM_011540045.1:c.7204G=	XP_011538347.1:p.Asp2402=
XM_011540046.1:c.6664G=	XP_011538348.1:p.Asp2222=
XM_011540047.1:c.6022G=	XP_011538349.1:p.Asp2008=
XM_011540052.1:c.3532G=	XP_011538354.1:p.Asp1178=
NM_022124.6:c.7009G= MANE Select	NP_071407.4:p.Asp2337=