Canonical Allele Identifier: CA470062527

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73562813A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71803056A>G , CM000672.2:g.71803056A>G	GRCh38
NC_000010.10:g.73562813A>G , CM000672.1:g.73562813A>G	GRCh37
NC_000010.9:g.73232819A>G	NCBI36
NG_008835.1:g.411110A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7641A>G MANE Select	ENSP00000224721.9:p.Ser2547=
ENST00000642965.1:c.1574A>G	ENSP00000495222.1:n.1574A>G
ENST00000647092.1:c.1238A>G	ENSP00000495176.1:n.1238A>G
ENST00000224721.10:c.7656A>G	ENSP00000224721.8:p.Ser2552=
ENST00000398788.4:c.921A>G	ENSP00000381768.3:p.Ser307=
ENST00000475158.1:n.1177A>G
ENST00000619887.4:c.921A>G	ENSP00000478374.1:p.Ser307=
ENST00000622827.4:c.7641A>G	ENSP00000483211.1:p.Ser2547=
NM_001171933.1:c.921A>G	NP_001165404.1:p.Ser307=
NM_001171934.1:c.921A>G	NP_001165405.1:p.Ser307=
NM_022124.5:c.7641A>G	NP_071407.4:p.Ser2547=
XM_006717940.2:c.7836A>G	XP_006718003.1:p.Ser2612=
XM_006717942.2:c.7770A>G	XP_006718005.1:p.Ser2590=
XM_011540039.1:c.7833A>G	XP_011538341.1:p.Ser2611=
XM_011540040.1:c.7830A>G	XP_011538342.1:p.Ser2610=
XM_011540041.1:c.7776A>G	XP_011538343.1:p.Ser2592=
XM_011540042.1:c.7746A>G	XP_011538344.1:p.Ser2582=
XM_011540043.1:c.7836A>G	XP_011538345.1:p.Ser2612=
XM_011540044.1:c.7701A>G	XP_011538346.1:p.Ser2567=
XM_011540045.1:c.7836A>G	XP_011538347.1:p.Ser2612=
XM_011540046.1:c.7296A>G	XP_011538348.1:p.Ser2432=
XM_011540047.1:c.6654A>G	XP_011538349.1:p.Ser2218=
XM_011540052.1:c.4164A>G	XP_011538354.1:p.Ser1388=
NM_022124.6:c.7641A>G MANE Select	NP_071407.4:p.Ser2547=