Canonical Allele Identifier: CA1918878513

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798578G= , CM000672.2:g.71798578G=	GRCh38
NC_000010.10:g.73558335G= , CM000672.1:g.73558335G=	GRCh37
NC_000010.9:g.73228341G=	NCBI36
NG_008835.1:g.406632G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7054G= MANE Select	ENSP00000224721.9:p.Gly2352=
ENST00000642965.1:c.987G=	ENSP00000495222.1:n.987G=
ENST00000647092.1:c.651G=	ENSP00000495176.1:n.651G=
ENST00000224721.10:c.7069G=	ENSP00000224721.8:p.Gly2357=
ENST00000398788.4:c.334G=	ENSP00000381768.3:p.Gly112=
ENST00000475158.1:n.590G=
ENST00000619887.4:c.334G=	ENSP00000478374.1:p.Gly112=
ENST00000622827.4:c.7054G=	ENSP00000483211.1:p.Gly2352=
NM_001171933.1:c.334G=	NP_001165404.1:p.Gly112=
NM_001171934.1:c.334G=	NP_001165405.1:p.Gly112=
NM_022124.5:c.7054G=	NP_071407.4:p.Gly2352=
XM_006717940.2:c.7249G=	XP_006718003.1:p.Gly2417=
XM_006717942.2:c.7183G=	XP_006718005.1:p.Gly2395=
XM_011540039.1:c.7246G=	XP_011538341.1:p.Gly2416=
XM_011540040.1:c.7243G=	XP_011538342.1:p.Gly2415=
XM_011540041.1:c.7189G=	XP_011538343.1:p.Gly2397=
XM_011540042.1:c.7159G=	XP_011538344.1:p.Gly2387=
XM_011540043.1:c.7249G=	XP_011538345.1:p.Gly2417=
XM_011540044.1:c.7114G=	XP_011538346.1:p.Gly2372=
XM_011540045.1:c.7249G=	XP_011538347.1:p.Gly2417=
XM_011540046.1:c.6709G=	XP_011538348.1:p.Gly2237=
XM_011540047.1:c.6067G=	XP_011538349.1:p.Gly2023=
XM_011540052.1:c.3577G=	XP_011538354.1:p.Gly1193=
NM_022124.6:c.7054G= MANE Select	NP_071407.4:p.Gly2352=