Canonical Allele Identifier: CA1918886619

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807671G= , CM000672.2:g.71807671G=	GRCh38
NC_000010.10:g.73567428G= , CM000672.1:g.73567428G=	GRCh37
NC_000010.9:g.73237434G=	NCBI36
NG_008835.1:g.415725G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8464G= MANE Select	ENSP00000224721.9:p.Asp2822=
ENST00000642965.1:c.2397G=	ENSP00000495222.1:n.2397G=
ENST00000647092.1:c.2061G=	ENSP00000495176.1:n.2061G=
ENST00000224721.10:c.8479G=	ENSP00000224721.8:p.Asp2827=
ENST00000398788.4:c.1744G=	ENSP00000381768.3:p.Asp582=
ENST00000475158.1:n.2000G=
ENST00000619887.4:c.1744G=	ENSP00000478374.1:p.Asp582=
ENST00000622827.4:c.8464G=	ENSP00000483211.1:p.Asp2822=
NM_001171933.1:c.1744G=	NP_001165404.1:p.Asp582=
NM_001171934.1:c.1744G=	NP_001165405.1:p.Asp582=
NM_022124.5:c.8464G=	NP_071407.4:p.Asp2822=
XM_006717940.2:c.8659G=	XP_006718003.1:p.Asp2887=
XM_006717942.2:c.8593G=	XP_006718005.1:p.Asp2865=
XM_011540039.1:c.8656G=	XP_011538341.1:p.Asp2886=
XM_011540040.1:c.8653G=	XP_011538342.1:p.Asp2885=
XM_011540041.1:c.8599G=	XP_011538343.1:p.Asp2867=
XM_011540042.1:c.8569G=	XP_011538344.1:p.Asp2857=
XM_011540043.1:c.8659G=	XP_011538345.1:p.Asp2887=
XM_011540044.1:c.8524G=	XP_011538346.1:p.Asp2842=
XM_011540045.1:c.8659G=	XP_011538347.1:p.Asp2887=
XM_011540046.1:c.8119G=	XP_011538348.1:p.Asp2707=
XM_011540047.1:c.7477G=	XP_011538349.1:p.Asp2493=
XM_011540052.1:c.4987G=	XP_011538354.1:p.Asp1663=
NM_022124.6:c.8464G= MANE Select	NP_071407.4:p.Asp2822=