Canonical Allele Identifier: CA470282092

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73559302C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799545C>G , CM000672.2:g.71799545C>G	GRCh38
NC_000010.10:g.73559302C>G , CM000672.1:g.73559302C>G	GRCh37
NC_000010.9:g.73229308C>G	NCBI36
NG_008835.1:g.407599C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7278C>G MANE Select	ENSP00000224721.9:p.Ala2426=
ENST00000642965.1:c.1211C>G	ENSP00000495222.1:n.1211C>G
ENST00000647092.1:c.875C>G	ENSP00000495176.1:n.875C>G
ENST00000224721.10:c.7293C>G	ENSP00000224721.8:p.Ala2431=
ENST00000398788.4:c.558C>G	ENSP00000381768.3:p.Ala186=
ENST00000475158.1:n.814C>G
ENST00000619887.4:c.558C>G	ENSP00000478374.1:p.Ala186=
ENST00000622827.4:c.7278C>G	ENSP00000483211.1:p.Ala2426=
NM_001171933.1:c.558C>G	NP_001165404.1:p.Ala186=
NM_001171934.1:c.558C>G	NP_001165405.1:p.Ala186=
NM_022124.5:c.7278C>G	NP_071407.4:p.Ala2426=
XM_006717940.2:c.7473C>G	XP_006718003.1:p.Ala2491=
XM_006717942.2:c.7407C>G	XP_006718005.1:p.Ala2469=
XM_011540039.1:c.7470C>G	XP_011538341.1:p.Ala2490=
XM_011540040.1:c.7467C>G	XP_011538342.1:p.Ala2489=
XM_011540041.1:c.7413C>G	XP_011538343.1:p.Ala2471=
XM_011540042.1:c.7383C>G	XP_011538344.1:p.Ala2461=
XM_011540043.1:c.7473C>G	XP_011538345.1:p.Ala2491=
XM_011540044.1:c.7338C>G	XP_011538346.1:p.Ala2446=
XM_011540045.1:c.7473C>G	XP_011538347.1:p.Ala2491=
XM_011540046.1:c.6933C>G	XP_011538348.1:p.Ala2311=
XM_011540047.1:c.6291C>G	XP_011538349.1:p.Ala2097=
XM_011540052.1:c.3801C>G	XP_011538354.1:p.Ala1267=
NM_022124.6:c.7278C>G MANE Select	NP_071407.4:p.Ala2426=