Canonical Allele Identifier: CA1918878422

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798393C= , CM000672.2:g.71798393C=	GRCh38
NC_000010.10:g.73558150C= , CM000672.1:g.73558150C=	GRCh37
NC_000010.9:g.73228156C=	NCBI36
NG_008835.1:g.406447C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6869C= MANE Select	ENSP00000224721.9:p.Thr2290=
ENST00000642965.1:c.802C=	ENSP00000495222.1:n.802C=
ENST00000647092.1:c.466C=	ENSP00000495176.1:n.466C=
ENST00000224721.10:c.6884C=	ENSP00000224721.8:p.Thr2295=
ENST00000398788.4:c.149C=	ENSP00000381768.3:p.Thr50=
ENST00000475158.1:n.405C=
ENST00000619887.4:c.149C=	ENSP00000478374.1:p.Thr50=
ENST00000622827.4:c.6869C=	ENSP00000483211.1:p.Thr2290=
NM_001171933.1:c.149C=	NP_001165404.1:p.Thr50=
NM_001171934.1:c.149C=	NP_001165405.1:p.Thr50=
NM_022124.5:c.6869C=	NP_071407.4:p.Thr2290=
XM_006717940.2:c.7064C=	XP_006718003.1:p.Thr2355=
XM_006717942.2:c.6998C=	XP_006718005.1:p.Thr2333=
XM_011540039.1:c.7061C=	XP_011538341.1:p.Thr2354=
XM_011540040.1:c.7058C=	XP_011538342.1:p.Thr2353=
XM_011540041.1:c.7004C=	XP_011538343.1:p.Thr2335=
XM_011540042.1:c.6974C=	XP_011538344.1:p.Thr2325=
XM_011540043.1:c.7064C=	XP_011538345.1:p.Thr2355=
XM_011540044.1:c.6929C=	XP_011538346.1:p.Thr2310=
XM_011540045.1:c.7064C=	XP_011538347.1:p.Thr2355=
XM_011540046.1:c.6524C=	XP_011538348.1:p.Thr2175=
XM_011540047.1:c.5882C=	XP_011538349.1:p.Thr1961=
XM_011540052.1:c.3392C=	XP_011538354.1:p.Thr1131=
NM_022124.6:c.6869C= MANE Select	NP_071407.4:p.Thr2290=