Canonical Allele Identifier: CA470062027

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558211C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798454C>G , CM000672.2:g.71798454C>G	GRCh38
NC_000010.10:g.73558211C>G , CM000672.1:g.73558211C>G	GRCh37
NC_000010.9:g.73228217C>G	NCBI36
NG_008835.1:g.406508C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6930C>G MANE Select	ENSP00000224721.9:p.Thr2310=
ENST00000642965.1:c.863C>G	ENSP00000495222.1:n.863C>G
ENST00000647092.1:c.527C>G	ENSP00000495176.1:n.527C>G
ENST00000224721.10:c.6945C>G	ENSP00000224721.8:p.Thr2315=
ENST00000398788.4:c.210C>G	ENSP00000381768.3:p.Thr70=
ENST00000475158.1:n.466C>G
ENST00000619887.4:c.210C>G	ENSP00000478374.1:p.Thr70=
ENST00000622827.4:c.6930C>G	ENSP00000483211.1:p.Thr2310=
NM_001171933.1:c.210C>G	NP_001165404.1:p.Thr70=
NM_001171934.1:c.210C>G	NP_001165405.1:p.Thr70=
NM_022124.5:c.6930C>G	NP_071407.4:p.Thr2310=
XM_006717940.2:c.7125C>G	XP_006718003.1:p.Thr2375=
XM_006717942.2:c.7059C>G	XP_006718005.1:p.Thr2353=
XM_011540039.1:c.7122C>G	XP_011538341.1:p.Thr2374=
XM_011540040.1:c.7119C>G	XP_011538342.1:p.Thr2373=
XM_011540041.1:c.7065C>G	XP_011538343.1:p.Thr2355=
XM_011540042.1:c.7035C>G	XP_011538344.1:p.Thr2345=
XM_011540043.1:c.7125C>G	XP_011538345.1:p.Thr2375=
XM_011540044.1:c.6990C>G	XP_011538346.1:p.Thr2330=
XM_011540045.1:c.7125C>G	XP_011538347.1:p.Thr2375=
XM_011540046.1:c.6585C>G	XP_011538348.1:p.Thr2195=
XM_011540047.1:c.5943C>G	XP_011538349.1:p.Thr1981=
XM_011540052.1:c.3453C>G	XP_011538354.1:p.Thr1151=
NM_022124.6:c.6930C>G MANE Select	NP_071407.4:p.Thr2310=