Canonical Allele Identifier: CA1918886607

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807667C= , CM000672.2:g.71807667C=	GRCh38
NC_000010.10:g.73567424C= , CM000672.1:g.73567424C=	GRCh37
NC_000010.9:g.73237430C=	NCBI36
NG_008835.1:g.415721C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8460C= MANE Select	ENSP00000224721.9:p.Thr2820=
ENST00000642965.1:c.2393C=	ENSP00000495222.1:n.2393C=
ENST00000647092.1:c.2057C=	ENSP00000495176.1:n.2057C=
ENST00000224721.10:c.8475C=	ENSP00000224721.8:p.Thr2825=
ENST00000398788.4:c.1740C=	ENSP00000381768.3:p.Thr580=
ENST00000475158.1:n.1996C=
ENST00000619887.4:c.1740C=	ENSP00000478374.1:p.Thr580=
ENST00000622827.4:c.8460C=	ENSP00000483211.1:p.Thr2820=
NM_001171933.1:c.1740C=	NP_001165404.1:p.Thr580=
NM_001171934.1:c.1740C=	NP_001165405.1:p.Thr580=
NM_022124.5:c.8460C=	NP_071407.4:p.Thr2820=
XM_006717940.2:c.8655C=	XP_006718003.1:p.Thr2885=
XM_006717942.2:c.8589C=	XP_006718005.1:p.Thr2863=
XM_011540039.1:c.8652C=	XP_011538341.1:p.Thr2884=
XM_011540040.1:c.8649C=	XP_011538342.1:p.Thr2883=
XM_011540041.1:c.8595C=	XP_011538343.1:p.Thr2865=
XM_011540042.1:c.8565C=	XP_011538344.1:p.Thr2855=
XM_011540043.1:c.8655C=	XP_011538345.1:p.Thr2885=
XM_011540044.1:c.8520C=	XP_011538346.1:p.Thr2840=
XM_011540045.1:c.8655C=	XP_011538347.1:p.Thr2885=
XM_011540046.1:c.8115C=	XP_011538348.1:p.Thr2705=
XM_011540047.1:c.7473C=	XP_011538349.1:p.Thr2491=
XM_011540052.1:c.4983C=	XP_011538354.1:p.Thr1661=
NM_022124.6:c.8460C= MANE Select	NP_071407.4:p.Thr2820=