Canonical Allele Identifier: CA1918880422

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71802989G= , CM000672.2:g.71802989G=	GRCh38
NC_000010.10:g.73562746G= , CM000672.1:g.73562746G=	GRCh37
NC_000010.9:g.73232752G=	NCBI36
NG_008835.1:g.411043G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7574G= MANE Select	ENSP00000224721.9:p.Gly2525=
ENST00000642965.1:c.1507G=	ENSP00000495222.1:n.1507G=
ENST00000647092.1:c.1171G=	ENSP00000495176.1:n.1171G=
ENST00000224721.10:c.7589G=	ENSP00000224721.8:p.Gly2530=
ENST00000398788.4:c.854G=	ENSP00000381768.3:p.Gly285=
ENST00000475158.1:n.1110G=
ENST00000619887.4:c.854G=	ENSP00000478374.1:p.Gly285=
ENST00000622827.4:c.7574G=	ENSP00000483211.1:p.Gly2525=
NM_001171933.1:c.854G=	NP_001165404.1:p.Gly285=
NM_001171934.1:c.854G=	NP_001165405.1:p.Gly285=
NM_022124.5:c.7574G=	NP_071407.4:p.Gly2525=
XM_006717940.2:c.7769G=	XP_006718003.1:p.Gly2590=
XM_006717942.2:c.7703G=	XP_006718005.1:p.Gly2568=
XM_011540039.1:c.7766G=	XP_011538341.1:p.Gly2589=
XM_011540040.1:c.7763G=	XP_011538342.1:p.Gly2588=
XM_011540041.1:c.7709G=	XP_011538343.1:p.Gly2570=
XM_011540042.1:c.7679G=	XP_011538344.1:p.Gly2560=
XM_011540043.1:c.7769G=	XP_011538345.1:p.Gly2590=
XM_011540044.1:c.7634G=	XP_011538346.1:p.Gly2545=
XM_011540045.1:c.7769G=	XP_011538347.1:p.Gly2590=
XM_011540046.1:c.7229G=	XP_011538348.1:p.Gly2410=
XM_011540047.1:c.6587G=	XP_011538349.1:p.Gly2196=
XM_011540052.1:c.4097G=	XP_011538354.1:p.Gly1366=
NM_022124.6:c.7574G= MANE Select	NP_071407.4:p.Gly2525=