Canonical Allele Identifier: CA1918880420

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71802985G= , CM000672.2:g.71802985G=	GRCh38
NC_000010.10:g.73562742G= , CM000672.1:g.73562742G=	GRCh37
NC_000010.9:g.73232748G=	NCBI36
NG_008835.1:g.411039G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7570G= MANE Select	ENSP00000224721.9:p.Ala2524=
ENST00000642965.1:c.1503G=	ENSP00000495222.1:n.1503G=
ENST00000647092.1:c.1167G=	ENSP00000495176.1:n.1167G=
ENST00000224721.10:c.7585G=	ENSP00000224721.8:p.Ala2529=
ENST00000398788.4:c.850G=	ENSP00000381768.3:p.Ala284=
ENST00000475158.1:n.1106G=
ENST00000619887.4:c.850G=	ENSP00000478374.1:p.Ala284=
ENST00000622827.4:c.7570G=	ENSP00000483211.1:p.Ala2524=
NM_001171933.1:c.850G=	NP_001165404.1:p.Ala284=
NM_001171934.1:c.850G=	NP_001165405.1:p.Ala284=
NM_022124.5:c.7570G=	NP_071407.4:p.Ala2524=
XM_006717940.2:c.7765G=	XP_006718003.1:p.Ala2589=
XM_006717942.2:c.7699G=	XP_006718005.1:p.Ala2567=
XM_011540039.1:c.7762G=	XP_011538341.1:p.Ala2588=
XM_011540040.1:c.7759G=	XP_011538342.1:p.Ala2587=
XM_011540041.1:c.7705G=	XP_011538343.1:p.Ala2569=
XM_011540042.1:c.7675G=	XP_011538344.1:p.Ala2559=
XM_011540043.1:c.7765G=	XP_011538345.1:p.Ala2589=
XM_011540044.1:c.7630G=	XP_011538346.1:p.Ala2544=
XM_011540045.1:c.7765G=	XP_011538347.1:p.Ala2589=
XM_011540046.1:c.7225G=	XP_011538348.1:p.Ala2409=
XM_011540047.1:c.6583G=	XP_011538349.1:p.Ala2195=
XM_011540052.1:c.4093G=	XP_011538354.1:p.Ala1365=
NM_022124.6:c.7570G= MANE Select	NP_071407.4:p.Ala2524=