Canonical Allele Identifier: CA2677794754
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944559_29944572del , CM000668.2:g.29944559_29944572del GRCh38
NC_000006.11:g.29912336_29912349del , CM000668.1:g.29912336_29912349del GRCh37
NC_000006.10:g.30020315_30020328del NCBI36
NG_029217.2:g.7095_7108del

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.895+162_895+175del ENSP00000492789.2:n.895+162_895+175del
ENST00000706892.1:n.1911_1924del
ENST00000706893.1:c.989_1002del ENSP00000516609.1:p.Trp330LeufsTer8
ENST00000706894.1:c.955_968del ENSP00000516610.1:p.Gly319TrpfsTer16
ENST00000706895.1:n.1333_1346del
ENST00000706896.1:n.1809_1822del
ENST00000706897.1:n.1231_1244del
ENST00000706898.1:c.955_968del ENSP00000516611.1:p.Gly319TrpfsTer22
ENST00000706899.1:n.1809_1822del
ENST00000706900.1:c.871_884del ENSP00000516617.1:p.Gly291TrpfsTer16
ENST00000706901.1:c.955_968del ENSP00000516612.1:p.Gly319TrpfsTer16
ENST00000706902.1:c.955_968del ENSP00000516613.1:p.Gly319TrpfsTer16
ENST00000706903.1:c.955_968del ENSP00000516614.1:p.Gly319TrpfsTer16
ENST00000706904.1:c.955_968del ENSP00000516615.1:p.Gly319TrpfsTer16
ENST00000706905.1:c.955_968del ENSP00000516616.1:p.Gly319TrpfsTer16
ENST00000376809.10:c.955_968del MANE Select ENSP00000366005.5:p.Gly319TrpfsTer16
ENST00000638375.1:c.895+162_895+175del ENSP00000492789.1:n.895+162_895+175del
ENST00000376802.2:c.895+162_895+175del ENSP00000365998.2:n.895+162_895+175del
ENST00000376806.9:c.955_968del ENSP00000366002.5:p.Gly319TrpfsTer22
ENST00000376809.9:c.955_968del ENSP00000366005.5:p.Gly319TrpfsTer16
ENST00000396634.5:c.955_968del ENSP00000379873.1:p.Gly319TrpfsTer16
ENST00000461903.1:n.1196_1209del
ENST00000479320.5:n.1196_1209del
ENST00000495183.5:n.1198_1211del
ENST00000496081.5:n.772_785del
NM_002116.7:c.955_968del NP_002107.3:p.Gly319TrpfsTer16
NM_002116.8:c.955_968del MANE Select NP_002107.3:p.Gly319TrpfsTer16