Canonical Allele Identifier: CA1918886456

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807519G= , CM000672.2:g.71807519G=	GRCh38
NC_000010.10:g.73567276G= , CM000672.1:g.73567276G=	GRCh37
NC_000010.9:g.73237282G=	NCBI36
NG_008835.1:g.415573G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8312G= MANE Select	ENSP00000224721.9:p.Gly2771=
ENST00000642965.1:c.2245G=	ENSP00000495222.1:n.2245G=
ENST00000647092.1:c.1909G=	ENSP00000495176.1:n.1909G=
ENST00000224721.10:c.8327G=	ENSP00000224721.8:p.Gly2776=
ENST00000398788.4:c.1592G=	ENSP00000381768.3:p.Gly531=
ENST00000475158.1:n.1848G=
ENST00000619887.4:c.1592G=	ENSP00000478374.1:p.Gly531=
ENST00000622827.4:c.8312G=	ENSP00000483211.1:p.Gly2771=
NM_001171933.1:c.1592G=	NP_001165404.1:p.Gly531=
NM_001171934.1:c.1592G=	NP_001165405.1:p.Gly531=
NM_022124.5:c.8312G=	NP_071407.4:p.Gly2771=
XM_006717940.2:c.8507G=	XP_006718003.1:p.Gly2836=
XM_006717942.2:c.8441G=	XP_006718005.1:p.Gly2814=
XM_011540039.1:c.8504G=	XP_011538341.1:p.Gly2835=
XM_011540040.1:c.8501G=	XP_011538342.1:p.Gly2834=
XM_011540041.1:c.8447G=	XP_011538343.1:p.Gly2816=
XM_011540042.1:c.8417G=	XP_011538344.1:p.Gly2806=
XM_011540043.1:c.8507G=	XP_011538345.1:p.Gly2836=
XM_011540044.1:c.8372G=	XP_011538346.1:p.Gly2791=
XM_011540045.1:c.8507G=	XP_011538347.1:p.Gly2836=
XM_011540046.1:c.7967G=	XP_011538348.1:p.Gly2656=
XM_011540047.1:c.7325G=	XP_011538349.1:p.Gly2442=
XM_011540052.1:c.4835G=	XP_011538354.1:p.Gly1612=
NM_022124.6:c.8312G= MANE Select	NP_071407.4:p.Gly2771=