Canonical Allele Identifier: CA2677794788
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944571_29944572del , CM000668.2:g.29944571_29944572del GRCh38
NC_000006.11:g.29912348_29912349del , CM000668.1:g.29912348_29912349del GRCh37
NC_000006.10:g.30020327_30020328del NCBI36
NG_029217.2:g.7107_7108del

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.895+174_895+175del ENSP00000492789.2:n.895+174_895+175del
ENST00000706892.1:n.1923_1924del
ENST00000706893.1:c.1001_1002del ENSP00000516609.1:p.His334LeufsTer8
ENST00000706894.1:c.967_968del ENSP00000516610.1:p.Thr323TrpfsTer16
ENST00000706895.1:n.1345_1346del
ENST00000706896.1:n.1821_1822del
ENST00000706897.1:n.1243_1244del
ENST00000706898.1:c.967_968del ENSP00000516611.1:p.Thr323TrpfsTer22
ENST00000706899.1:n.1821_1822del
ENST00000706900.1:c.883_884del ENSP00000516617.1:p.Thr295TrpfsTer16
ENST00000706901.1:c.967_968del ENSP00000516612.1:p.Thr323TrpfsTer16
ENST00000706902.1:c.967_968del ENSP00000516613.1:p.Thr323TrpfsTer16
ENST00000706903.1:c.967_968del ENSP00000516614.1:p.Thr323TrpfsTer16
ENST00000706904.1:c.967_968del ENSP00000516615.1:p.Thr323TrpfsTer16
ENST00000706905.1:c.967_968del ENSP00000516616.1:p.Thr323TrpfsTer16
ENST00000376809.10:c.967_968del MANE Select ENSP00000366005.5:p.Thr323TrpfsTer16
ENST00000638375.1:c.895+174_895+175del ENSP00000492789.1:n.895+174_895+175del
ENST00000376802.2:c.895+174_895+175del ENSP00000365998.2:n.895+174_895+175del
ENST00000376806.9:c.967_968del ENSP00000366002.5:p.Thr323TrpfsTer22
ENST00000376809.9:c.967_968del ENSP00000366005.5:p.Thr323TrpfsTer16
ENST00000396634.5:c.967_968del ENSP00000379873.1:p.Thr323TrpfsTer16
ENST00000461903.1:n.1208_1209del
ENST00000479320.5:n.1208_1209del
ENST00000495183.5:n.1210_1211del
ENST00000496081.5:n.784_785del
NM_002116.7:c.967_968del NP_002107.3:p.Thr323TrpfsTer16
NM_002116.8:c.967_968del MANE Select NP_002107.3:p.Thr323TrpfsTer16