Canonical Allele Identifier: CA1918886543

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807606C= , CM000672.2:g.71807606C=	GRCh38
NC_000010.10:g.73567363C= , CM000672.1:g.73567363C=	GRCh37
NC_000010.9:g.73237369C=	NCBI36
NG_008835.1:g.415660C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8399C= MANE Select	ENSP00000224721.9:p.Ser2800=
ENST00000642965.1:c.2332C=	ENSP00000495222.1:n.2332C=
ENST00000647092.1:c.1996C=	ENSP00000495176.1:n.1996C=
ENST00000224721.10:c.8414C=	ENSP00000224721.8:p.Ser2805=
ENST00000398788.4:c.1679C=	ENSP00000381768.3:p.Ser560=
ENST00000475158.1:n.1935C=
ENST00000619887.4:c.1679C=	ENSP00000478374.1:p.Ser560=
ENST00000622827.4:c.8399C=	ENSP00000483211.1:p.Ser2800=
NM_001171933.1:c.1679C=	NP_001165404.1:p.Ser560=
NM_001171934.1:c.1679C=	NP_001165405.1:p.Ser560=
NM_022124.5:c.8399C=	NP_071407.4:p.Ser2800=
XM_006717940.2:c.8594C=	XP_006718003.1:p.Ser2865=
XM_006717942.2:c.8528C=	XP_006718005.1:p.Ser2843=
XM_011540039.1:c.8591C=	XP_011538341.1:p.Ser2864=
XM_011540040.1:c.8588C=	XP_011538342.1:p.Ser2863=
XM_011540041.1:c.8534C=	XP_011538343.1:p.Ser2845=
XM_011540042.1:c.8504C=	XP_011538344.1:p.Ser2835=
XM_011540043.1:c.8594C=	XP_011538345.1:p.Ser2865=
XM_011540044.1:c.8459C=	XP_011538346.1:p.Ser2820=
XM_011540045.1:c.8594C=	XP_011538347.1:p.Ser2865=
XM_011540046.1:c.8054C=	XP_011538348.1:p.Ser2685=
XM_011540047.1:c.7412C=	XP_011538349.1:p.Ser2471=
XM_011540052.1:c.4922C=	XP_011538354.1:p.Ser1641=
NM_022124.6:c.8399C= MANE Select	NP_071407.4:p.Ser2800=