Canonical Allele Identifier: CA1918886554

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807617A= , CM000672.2:g.71807617A=	GRCh38
NC_000010.10:g.73567374A= , CM000672.1:g.73567374A=	GRCh37
NC_000010.9:g.73237380A=	NCBI36
NG_008835.1:g.415671A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8410A= MANE Select	ENSP00000224721.9:p.Lys2804=
ENST00000642965.1:c.2343A=	ENSP00000495222.1:n.2343A=
ENST00000647092.1:c.2007A=	ENSP00000495176.1:n.2007A=
ENST00000224721.10:c.8425A=	ENSP00000224721.8:p.Lys2809=
ENST00000398788.4:c.1690A=	ENSP00000381768.3:p.Lys564=
ENST00000475158.1:n.1946A=
ENST00000619887.4:c.1690A=	ENSP00000478374.1:p.Lys564=
ENST00000622827.4:c.8410A=	ENSP00000483211.1:p.Lys2804=
NM_001171933.1:c.1690A=	NP_001165404.1:p.Lys564=
NM_001171934.1:c.1690A=	NP_001165405.1:p.Lys564=
NM_022124.5:c.8410A=	NP_071407.4:p.Lys2804=
XM_006717940.2:c.8605A=	XP_006718003.1:p.Lys2869=
XM_006717942.2:c.8539A=	XP_006718005.1:p.Lys2847=
XM_011540039.1:c.8602A=	XP_011538341.1:p.Lys2868=
XM_011540040.1:c.8599A=	XP_011538342.1:p.Lys2867=
XM_011540041.1:c.8545A=	XP_011538343.1:p.Lys2849=
XM_011540042.1:c.8515A=	XP_011538344.1:p.Lys2839=
XM_011540043.1:c.8605A=	XP_011538345.1:p.Lys2869=
XM_011540044.1:c.8470A=	XP_011538346.1:p.Lys2824=
XM_011540045.1:c.8605A=	XP_011538347.1:p.Lys2869=
XM_011540046.1:c.8065A=	XP_011538348.1:p.Lys2689=
XM_011540047.1:c.7423A=	XP_011538349.1:p.Lys2475=
XM_011540052.1:c.4933A=	XP_011538354.1:p.Lys1645=
NM_022124.6:c.8410A= MANE Select	NP_071407.4:p.Lys2804=