Canonical Allele Identifier: CA1918878921

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799541C= , CM000672.2:g.71799541C=	GRCh38
NC_000010.10:g.73559298C= , CM000672.1:g.73559298C=	GRCh37
NC_000010.9:g.73229304C=	NCBI36
NG_008835.1:g.407595C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7274C= MANE Select	ENSP00000224721.9:p.Thr2425=
ENST00000642965.1:c.1207C=	ENSP00000495222.1:n.1207C=
ENST00000647092.1:c.871C=	ENSP00000495176.1:n.871C=
ENST00000224721.10:c.7289C=	ENSP00000224721.8:p.Thr2430=
ENST00000398788.4:c.554C=	ENSP00000381768.3:p.Thr185=
ENST00000475158.1:n.810C=
ENST00000619887.4:c.554C=	ENSP00000478374.1:p.Thr185=
ENST00000622827.4:c.7274C=	ENSP00000483211.1:p.Thr2425=
NM_001171933.1:c.554C=	NP_001165404.1:p.Thr185=
NM_001171934.1:c.554C=	NP_001165405.1:p.Thr185=
NM_022124.5:c.7274C=	NP_071407.4:p.Thr2425=
XM_006717940.2:c.7469C=	XP_006718003.1:p.Thr2490=
XM_006717942.2:c.7403C=	XP_006718005.1:p.Thr2468=
XM_011540039.1:c.7466C=	XP_011538341.1:p.Thr2489=
XM_011540040.1:c.7463C=	XP_011538342.1:p.Thr2488=
XM_011540041.1:c.7409C=	XP_011538343.1:p.Thr2470=
XM_011540042.1:c.7379C=	XP_011538344.1:p.Thr2460=
XM_011540043.1:c.7469C=	XP_011538345.1:p.Thr2490=
XM_011540044.1:c.7334C=	XP_011538346.1:p.Thr2445=
XM_011540045.1:c.7469C=	XP_011538347.1:p.Thr2490=
XM_011540046.1:c.6929C=	XP_011538348.1:p.Thr2310=
XM_011540047.1:c.6287C=	XP_011538349.1:p.Thr2096=
XM_011540052.1:c.3797C=	XP_011538354.1:p.Thr1266=
NM_022124.6:c.7274C= MANE Select	NP_071407.4:p.Thr2425=