Canonical Allele Identifier: CA377157931

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558201A>T (hg19) ; chr10:g.71798444A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798444A>T , CM000672.2:g.71798444A>T	GRCh38
NC_000010.10:g.73558201A>T , CM000672.1:g.73558201A>T	GRCh37
NC_000010.9:g.73228207A>T	NCBI36
NG_008835.1:g.406498A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6920A>T MANE Select	ENSP00000224721.9:p.Glu2307Val
ENST00000642965.1:c.853A>T	ENSP00000495222.1:n.853A>T
ENST00000647092.1:c.517A>T	ENSP00000495176.1:n.517A>T
ENST00000224721.10:c.6935A>T	ENSP00000224721.8:p.Glu2312Val
ENST00000398788.4:c.200A>T	ENSP00000381768.3:p.Glu67Val
ENST00000475158.1:n.456A>T
ENST00000619887.4:c.200A>T	ENSP00000478374.1:p.Glu67Val
ENST00000622827.4:c.6920A>T	ENSP00000483211.1:p.Glu2307Val
NM_001171933.1:c.200A>T	NP_001165404.1:p.Glu67Val
NM_001171934.1:c.200A>T	NP_001165405.1:p.Glu67Val
NM_022124.5:c.6920A>T	NP_071407.4:p.Glu2307Val
XM_006717940.2:c.7115A>T	XP_006718003.1:p.Glu2372Val
XM_006717942.2:c.7049A>T	XP_006718005.1:p.Glu2350Val
XM_011540039.1:c.7112A>T	XP_011538341.1:p.Glu2371Val
XM_011540040.1:c.7109A>T	XP_011538342.1:p.Glu2370Val
XM_011540041.1:c.7055A>T	XP_011538343.1:p.Glu2352Val
XM_011540042.1:c.7025A>T	XP_011538344.1:p.Glu2342Val
XM_011540043.1:c.7115A>T	XP_011538345.1:p.Glu2372Val
XM_011540044.1:c.6980A>T	XP_011538346.1:p.Glu2327Val
XM_011540045.1:c.7115A>T	XP_011538347.1:p.Glu2372Val
XM_011540046.1:c.6575A>T	XP_011538348.1:p.Glu2192Val
XM_011540047.1:c.5933A>T	XP_011538349.1:p.Glu1978Val
XM_011540052.1:c.3443A>T	XP_011538354.1:p.Glu1148Val
NM_022124.6:c.6920A>T MANE Select	NP_071407.4:p.Glu2307Val