Canonical Allele Identifier: CA1918886561

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807623T= , CM000672.2:g.71807623T=	GRCh38
NC_000010.10:g.73567380T= , CM000672.1:g.73567380T=	GRCh37
NC_000010.9:g.73237386T=	NCBI36
NG_008835.1:g.415677T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8416T= MANE Select	ENSP00000224721.9:p.Ser2806=
ENST00000642965.1:c.2349T=	ENSP00000495222.1:n.2349T=
ENST00000647092.1:c.2013T=	ENSP00000495176.1:n.2013T=
ENST00000224721.10:c.8431T=	ENSP00000224721.8:p.Ser2811=
ENST00000398788.4:c.1696T=	ENSP00000381768.3:p.Ser566=
ENST00000475158.1:n.1952T=
ENST00000619887.4:c.1696T=	ENSP00000478374.1:p.Ser566=
ENST00000622827.4:c.8416T=	ENSP00000483211.1:p.Ser2806=
NM_001171933.1:c.1696T=	NP_001165404.1:p.Ser566=
NM_001171934.1:c.1696T=	NP_001165405.1:p.Ser566=
NM_022124.5:c.8416T=	NP_071407.4:p.Ser2806=
XM_006717940.2:c.8611T=	XP_006718003.1:p.Ser2871=
XM_006717942.2:c.8545T=	XP_006718005.1:p.Ser2849=
XM_011540039.1:c.8608T=	XP_011538341.1:p.Ser2870=
XM_011540040.1:c.8605T=	XP_011538342.1:p.Ser2869=
XM_011540041.1:c.8551T=	XP_011538343.1:p.Ser2851=
XM_011540042.1:c.8521T=	XP_011538344.1:p.Ser2841=
XM_011540043.1:c.8611T=	XP_011538345.1:p.Ser2871=
XM_011540044.1:c.8476T=	XP_011538346.1:p.Ser2826=
XM_011540045.1:c.8611T=	XP_011538347.1:p.Ser2871=
XM_011540046.1:c.8071T=	XP_011538348.1:p.Ser2691=
XM_011540047.1:c.7429T=	XP_011538349.1:p.Ser2477=
XM_011540052.1:c.4939T=	XP_011538354.1:p.Ser1647=
NM_022124.6:c.8416T= MANE Select	NP_071407.4:p.Ser2806=