Canonical Allele Identifier: CA1918886578

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807640G= , CM000672.2:g.71807640G=	GRCh38
NC_000010.10:g.73567397G= , CM000672.1:g.73567397G=	GRCh37
NC_000010.9:g.73237403G=	NCBI36
NG_008835.1:g.415694G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8433G= MANE Select	ENSP00000224721.9:p.Trp2811=
ENST00000642965.1:c.2366G=	ENSP00000495222.1:n.2366G=
ENST00000647092.1:c.2030G=	ENSP00000495176.1:n.2030G=
ENST00000224721.10:c.8448G=	ENSP00000224721.8:p.Trp2816=
ENST00000398788.4:c.1713G=	ENSP00000381768.3:p.Trp571=
ENST00000475158.1:n.1969G=
ENST00000619887.4:c.1713G=	ENSP00000478374.1:p.Trp571=
ENST00000622827.4:c.8433G=	ENSP00000483211.1:p.Trp2811=
NM_001171933.1:c.1713G=	NP_001165404.1:p.Trp571=
NM_001171934.1:c.1713G=	NP_001165405.1:p.Trp571=
NM_022124.5:c.8433G=	NP_071407.4:p.Trp2811=
XM_006717940.2:c.8628G=	XP_006718003.1:p.Trp2876=
XM_006717942.2:c.8562G=	XP_006718005.1:p.Trp2854=
XM_011540039.1:c.8625G=	XP_011538341.1:p.Trp2875=
XM_011540040.1:c.8622G=	XP_011538342.1:p.Trp2874=
XM_011540041.1:c.8568G=	XP_011538343.1:p.Trp2856=
XM_011540042.1:c.8538G=	XP_011538344.1:p.Trp2846=
XM_011540043.1:c.8628G=	XP_011538345.1:p.Trp2876=
XM_011540044.1:c.8493G=	XP_011538346.1:p.Trp2831=
XM_011540045.1:c.8628G=	XP_011538347.1:p.Trp2876=
XM_011540046.1:c.8088G=	XP_011538348.1:p.Trp2696=
XM_011540047.1:c.7446G=	XP_011538349.1:p.Trp2482=
XM_011540052.1:c.4956G=	XP_011538354.1:p.Trp1652=
NM_022124.6:c.8433G= MANE Select	NP_071407.4:p.Trp2811=