Canonical Allele Identifier: CA1918886545

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807608T= , CM000672.2:g.71807608T=	GRCh38
NC_000010.10:g.73567365T= , CM000672.1:g.73567365T=	GRCh37
NC_000010.9:g.73237371T=	NCBI36
NG_008835.1:g.415662T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8401T= MANE Select	ENSP00000224721.9:p.Phe2801=
ENST00000642965.1:c.2334T=	ENSP00000495222.1:n.2334T=
ENST00000647092.1:c.1998T=	ENSP00000495176.1:n.1998T=
ENST00000224721.10:c.8416T=	ENSP00000224721.8:p.Phe2806=
ENST00000398788.4:c.1681T=	ENSP00000381768.3:p.Phe561=
ENST00000475158.1:n.1937T=
ENST00000619887.4:c.1681T=	ENSP00000478374.1:p.Phe561=
ENST00000622827.4:c.8401T=	ENSP00000483211.1:p.Phe2801=
NM_001171933.1:c.1681T=	NP_001165404.1:p.Phe561=
NM_001171934.1:c.1681T=	NP_001165405.1:p.Phe561=
NM_022124.5:c.8401T=	NP_071407.4:p.Phe2801=
XM_006717940.2:c.8596T=	XP_006718003.1:p.Phe2866=
XM_006717942.2:c.8530T=	XP_006718005.1:p.Phe2844=
XM_011540039.1:c.8593T=	XP_011538341.1:p.Phe2865=
XM_011540040.1:c.8590T=	XP_011538342.1:p.Phe2864=
XM_011540041.1:c.8536T=	XP_011538343.1:p.Phe2846=
XM_011540042.1:c.8506T=	XP_011538344.1:p.Phe2836=
XM_011540043.1:c.8596T=	XP_011538345.1:p.Phe2866=
XM_011540044.1:c.8461T=	XP_011538346.1:p.Phe2821=
XM_011540045.1:c.8596T=	XP_011538347.1:p.Phe2866=
XM_011540046.1:c.8056T=	XP_011538348.1:p.Phe2686=
XM_011540047.1:c.7414T=	XP_011538349.1:p.Phe2472=
XM_011540052.1:c.4924T=	XP_011538354.1:p.Phe1642=
NM_022124.6:c.8401T= MANE Select	NP_071407.4:p.Phe2801=