Canonical Allele Identifier: CA1918878963

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799650T= , CM000672.2:g.71799650T=	GRCh38
NC_000010.10:g.73559407T= , CM000672.1:g.73559407T=	GRCh37
NC_000010.9:g.73229413T=	NCBI36
NG_008835.1:g.407704T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7362+21T= MANE Select	ENSP00000224721.9:n.7362+21T=
ENST00000642965.1:c.1295+21T=	ENSP00000495222.1:n.1295+21T=
ENST00000647092.1:c.959+21T=	ENSP00000495176.1:n.959+21T=
ENST00000224721.10:c.7377+21T=	ENSP00000224721.8:n.7377+21T=
ENST00000398788.4:c.642+21T=	ENSP00000381768.3:n.642+21T=
ENST00000475158.1:n.898+21T=
ENST00000619887.4:c.642+21T=	ENSP00000478374.1:n.642+21T=
ENST00000622827.4:c.7362+21T=	ENSP00000483211.1:n.7362+21T=
NM_001171933.1:c.642+21T=	NP_001165404.1:n.642+21T=
NM_001171934.1:c.642+21T=	NP_001165405.1:n.642+21T=
NM_022124.5:c.7362+21T=	NP_071407.4:n.7362+21T=
XM_006717940.2:c.7557+21T=	XP_006718003.1:n.7557+21T=
XM_006717942.2:c.7491+21T=	XP_006718005.1:n.7491+21T=
XM_011540039.1:c.7554+21T=	XP_011538341.1:n.7554+21T=
XM_011540040.1:c.7551+21T=	XP_011538342.1:n.7551+21T=
XM_011540041.1:c.7497+21T=	XP_011538343.1:n.7497+21T=
XM_011540042.1:c.7467+21T=	XP_011538344.1:n.7467+21T=
XM_011540043.1:c.7557+21T=	XP_011538345.1:n.7557+21T=
XM_011540044.1:c.7422+21T=	XP_011538346.1:n.7422+21T=
XM_011540045.1:c.7557+21T=	XP_011538347.1:n.7557+21T=
XM_011540046.1:c.7017+21T=	XP_011538348.1:n.7017+21T=
XM_011540047.1:c.6375+21T=	XP_011538349.1:n.6375+21T=
XM_011540052.1:c.3885+21T=	XP_011538354.1:n.3885+21T=
NM_022124.6:c.7362+21T= MANE Select	NP_071407.4:n.7362+21T=