Canonical Allele Identifier: CA1918878426

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798400G= , CM000672.2:g.71798400G=	GRCh38
NC_000010.10:g.73558157G= , CM000672.1:g.73558157G=	GRCh37
NC_000010.9:g.73228163G=	NCBI36
NG_008835.1:g.406454G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6876G= MANE Select	ENSP00000224721.9:p.Gln2292=
ENST00000642965.1:c.809G=	ENSP00000495222.1:n.809G=
ENST00000647092.1:c.473G=	ENSP00000495176.1:n.473G=
ENST00000224721.10:c.6891G=	ENSP00000224721.8:p.Gln2297=
ENST00000398788.4:c.156G=	ENSP00000381768.3:p.Gln52=
ENST00000475158.1:n.412G=
ENST00000619887.4:c.156G=	ENSP00000478374.1:p.Gln52=
ENST00000622827.4:c.6876G=	ENSP00000483211.1:p.Gln2292=
NM_001171933.1:c.156G=	NP_001165404.1:p.Gln52=
NM_001171934.1:c.156G=	NP_001165405.1:p.Gln52=
NM_022124.5:c.6876G=	NP_071407.4:p.Gln2292=
XM_006717940.2:c.7071G=	XP_006718003.1:p.Gln2357=
XM_006717942.2:c.7005G=	XP_006718005.1:p.Gln2335=
XM_011540039.1:c.7068G=	XP_011538341.1:p.Gln2356=
XM_011540040.1:c.7065G=	XP_011538342.1:p.Gln2355=
XM_011540041.1:c.7011G=	XP_011538343.1:p.Gln2337=
XM_011540042.1:c.6981G=	XP_011538344.1:p.Gln2327=
XM_011540043.1:c.7071G=	XP_011538345.1:p.Gln2357=
XM_011540044.1:c.6936G=	XP_011538346.1:p.Gln2312=
XM_011540045.1:c.7071G=	XP_011538347.1:p.Gln2357=
XM_011540046.1:c.6531G=	XP_011538348.1:p.Gln2177=
XM_011540047.1:c.5889G=	XP_011538349.1:p.Gln1963=
XM_011540052.1:c.3399G=	XP_011538354.1:p.Gln1133=
NM_022124.6:c.6876G= MANE Select	NP_071407.4:p.Gln2292=