Canonical Allele Identifier: CA1918878919

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799537G= , CM000672.2:g.71799537G=	GRCh38
NC_000010.10:g.73559294G= , CM000672.1:g.73559294G=	GRCh37
NC_000010.9:g.73229300G=	NCBI36
NG_008835.1:g.407591G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7270G= MANE Select	ENSP00000224721.9:p.Val2424=
ENST00000642965.1:c.1203G=	ENSP00000495222.1:n.1203G=
ENST00000647092.1:c.867G=	ENSP00000495176.1:n.867G=
ENST00000224721.10:c.7285G=	ENSP00000224721.8:p.Val2429=
ENST00000398788.4:c.550G=	ENSP00000381768.3:p.Val184=
ENST00000475158.1:n.806G=
ENST00000619887.4:c.550G=	ENSP00000478374.1:p.Val184=
ENST00000622827.4:c.7270G=	ENSP00000483211.1:p.Val2424=
NM_001171933.1:c.550G=	NP_001165404.1:p.Val184=
NM_001171934.1:c.550G=	NP_001165405.1:p.Val184=
NM_022124.5:c.7270G=	NP_071407.4:p.Val2424=
XM_006717940.2:c.7465G=	XP_006718003.1:p.Val2489=
XM_006717942.2:c.7399G=	XP_006718005.1:p.Val2467=
XM_011540039.1:c.7462G=	XP_011538341.1:p.Val2488=
XM_011540040.1:c.7459G=	XP_011538342.1:p.Val2487=
XM_011540041.1:c.7405G=	XP_011538343.1:p.Val2469=
XM_011540042.1:c.7375G=	XP_011538344.1:p.Val2459=
XM_011540043.1:c.7465G=	XP_011538345.1:p.Val2489=
XM_011540044.1:c.7330G=	XP_011538346.1:p.Val2444=
XM_011540045.1:c.7465G=	XP_011538347.1:p.Val2489=
XM_011540046.1:c.6925G=	XP_011538348.1:p.Val2309=
XM_011540047.1:c.6283G=	XP_011538349.1:p.Val2095=
XM_011540052.1:c.3793G=	XP_011538354.1:p.Val1265=
NM_022124.6:c.7270G= MANE Select	NP_071407.4:p.Val2424=