Canonical Allele Identifier: CA2770463955
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944154_29944155insGCTG , CM000668.2:g.29944154_29944155insGCTG GRCh38
NC_000006.11:g.29911931_29911932insGCTG , CM000668.1:g.29911931_29911932insGCTG GRCh37
NC_000006.10:g.30019910_30019911insGCTG NCBI36
NG_029217.2:g.6690_6691insGCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.652_653insGCTG ENSP00000492789.2:p.Ile218SerfsTer4
ENST00000706892.1:n.1506_1507insGCTG
ENST00000706893.1:c.652_653insGCTG ENSP00000516609.1:p.Ile218SerfsTer4
ENST00000706894.1:c.652_653insGCTG ENSP00000516610.1:p.Ile218SerfsTer4
ENST00000706895.1:n.928_929insGCTG
ENST00000706896.1:n.1506_1507insGCTG
ENST00000706897.1:n.928_929insGCTG
ENST00000706898.1:c.652_653insGCTG ENSP00000516611.1:p.Ile218SerfsTer4
ENST00000706899.1:n.1506_1507insGCTG
ENST00000706900.1:c.568_569insGCTG ENSP00000516617.1:p.Ile190SerfsTer4
ENST00000706901.1:c.652_653insGCTG ENSP00000516612.1:p.Ile218SerfsTer4
ENST00000706902.1:c.652_653insGCTG ENSP00000516613.1:p.Ile218SerfsTer4
ENST00000706903.1:c.652_653insGCTG ENSP00000516614.1:p.Ile218SerfsTer4
ENST00000706904.1:c.652_653insGCTG ENSP00000516615.1:p.Ile218SerfsTer4
ENST00000706905.1:c.652_653insGCTG ENSP00000516616.1:p.Ile218SerfsTer4
ENST00000376809.10:c.652_653insGCTG MANE Select ENSP00000366005.5:p.Ile218SerfsTer4
ENST00000638375.1:c.652_653insGCTG ENSP00000492789.1:p.Ile218SerfsTer4
ENST00000376802.2:c.652_653insGCTG ENSP00000365998.2:p.Ile218SerfsTer4
ENST00000376806.9:c.652_653insGCTG ENSP00000366002.5:p.Ile218SerfsTer4
ENST00000376809.9:c.652_653insGCTG ENSP00000366005.5:p.Ile218SerfsTer4
ENST00000396634.5:c.652_653insGCTG ENSP00000379873.1:p.Ile218SerfsTer4
ENST00000461903.1:n.893_894insGCTG
ENST00000479320.5:n.893_894insGCTG
ENST00000495183.5:n.895_896insGCTG
ENST00000496081.5:n.469_470insGCTG
NM_002116.7:c.652_653insGCTG NP_002107.3:p.Ile218SerfsTer4
NM_002116.8:c.652_653insGCTG MANE Select NP_002107.3:p.Ile218SerfsTer4