Canonical Allele Identifier: CA1087341453
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943452_29943453insTG , CM000668.2:g.29943452_29943453insTG GRCh38
NC_000006.11:g.29911229_29911230insTG , CM000668.1:g.29911229_29911230insTG GRCh37
NC_000006.10:g.30019208_30019209insTG NCBI36
NG_029217.2:g.5987_5988insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.528_529insTG ENSP00000492789.2:p.Ala177TrpfsTer5
ENST00000706892.1:n.804_805insTG
ENST00000706893.1:c.528_529insTG ENSP00000516609.1:p.Ala177TrpfsTer5
ENST00000706894.1:c.528_529insTG ENSP00000516610.1:p.Ala177TrpfsTer5
ENST00000706895.1:n.804_805insTG
ENST00000706896.1:n.804_805insTG
ENST00000706897.1:n.804_805insTG
ENST00000706898.1:c.528_529insTG ENSP00000516611.1:p.Ala177TrpfsTer5
ENST00000706899.1:n.804_805insTG
ENST00000706900.1:c.444_445insTG ENSP00000516617.1:p.Ala149TrpfsTer5
ENST00000706901.1:c.528_529insTG ENSP00000516612.1:p.Ala177TrpfsTer5
ENST00000706902.1:c.528_529insTG ENSP00000516613.1:p.Ala177TrpfsTer5
ENST00000706903.1:c.528_529insTG ENSP00000516614.1:p.Ala177TrpfsTer5
ENST00000706904.1:c.528_529insTG ENSP00000516615.1:p.Ala177TrpfsTer5
ENST00000706905.1:c.528_529insTG ENSP00000516616.1:p.Ala177TrpfsTer5
ENST00000376809.10:c.528_529insTG MANE Select ENSP00000366005.5:p.Ala177TrpfsTer5
ENST00000638375.1:c.528_529insTG ENSP00000492789.1:p.Ala177TrpfsTer5
ENST00000376802.2:c.528_529insTG ENSP00000365998.2:p.Ala177TrpfsTer5
ENST00000376806.9:c.528_529insTG ENSP00000366002.5:p.Ala177TrpfsTer5
ENST00000376809.9:c.528_529insTG ENSP00000366005.5:p.Ala177TrpfsTer5
ENST00000396634.5:c.528_529insTG ENSP00000379873.1:p.Ala177TrpfsTer5
ENST00000461903.1:n.769_770insTG
ENST00000479320.5:n.769_770insTG
ENST00000495183.5:n.771_772insTG
ENST00000496081.5:n.345_346insTG
NM_002116.7:c.528_529insTG NP_002107.3:p.Ala177TrpfsTer5
NM_002116.8:c.528_529insTG MANE Select NP_002107.3:p.Ala177TrpfsTer5