Canonical Allele Identifier: CA1918878456

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798463C= , CM000672.2:g.71798463C=	GRCh38
NC_000010.10:g.73558220C= , CM000672.1:g.73558220C=	GRCh37
NC_000010.9:g.73228226C=	NCBI36
NG_008835.1:g.406517C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6939C= MANE Select	ENSP00000224721.9:p.Thr2313=
ENST00000642965.1:c.872C=	ENSP00000495222.1:n.872C=
ENST00000647092.1:c.536C=	ENSP00000495176.1:n.536C=
ENST00000224721.10:c.6954C=	ENSP00000224721.8:p.Thr2318=
ENST00000398788.4:c.219C=	ENSP00000381768.3:p.Thr73=
ENST00000475158.1:n.475C=
ENST00000619887.4:c.219C=	ENSP00000478374.1:p.Thr73=
ENST00000622827.4:c.6939C=	ENSP00000483211.1:p.Thr2313=
NM_001171933.1:c.219C=	NP_001165404.1:p.Thr73=
NM_001171934.1:c.219C=	NP_001165405.1:p.Thr73=
NM_022124.5:c.6939C=	NP_071407.4:p.Thr2313=
XM_006717940.2:c.7134C=	XP_006718003.1:p.Thr2378=
XM_006717942.2:c.7068C=	XP_006718005.1:p.Thr2356=
XM_011540039.1:c.7131C=	XP_011538341.1:p.Thr2377=
XM_011540040.1:c.7128C=	XP_011538342.1:p.Thr2376=
XM_011540041.1:c.7074C=	XP_011538343.1:p.Thr2358=
XM_011540042.1:c.7044C=	XP_011538344.1:p.Thr2348=
XM_011540043.1:c.7134C=	XP_011538345.1:p.Thr2378=
XM_011540044.1:c.6999C=	XP_011538346.1:p.Thr2333=
XM_011540045.1:c.7134C=	XP_011538347.1:p.Thr2378=
XM_011540046.1:c.6594C=	XP_011538348.1:p.Thr2198=
XM_011540047.1:c.5952C=	XP_011538349.1:p.Thr1984=
XM_011540052.1:c.3462C=	XP_011538354.1:p.Thr1154=
NM_022124.6:c.6939C= MANE Select	NP_071407.4:p.Thr2313=