Canonical Allele Identifier: CA823768200
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs1211193467

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944128_29944129insGC , CM000668.2:g.29944128_29944129insGC GRCh38
NC_000006.11:g.29911905_29911906insGC , CM000668.1:g.29911905_29911906insGC GRCh37
NC_000006.10:g.30019884_30019885insGC NCBI36
NG_029217.2:g.6664_6665insGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.626_627insGC ENSP00000492789.2:p.Lys210ProfsTer5
ENST00000706892.1:n.1480_1481insGC
ENST00000706893.1:c.626_627insGC ENSP00000516609.1:p.Lys210ProfsTer5
ENST00000706894.1:c.626_627insGC ENSP00000516610.1:p.Lys210ProfsTer5
ENST00000706895.1:n.902_903insGC
ENST00000706896.1:n.1480_1481insGC
ENST00000706897.1:n.902_903insGC
ENST00000706898.1:c.626_627insGC ENSP00000516611.1:p.Lys210ProfsTer5
ENST00000706899.1:n.1480_1481insGC
ENST00000706900.1:c.542_543insGC ENSP00000516617.1:p.Lys182ProfsTer5
ENST00000706901.1:c.626_627insGC ENSP00000516612.1:p.Lys210ProfsTer5
ENST00000706902.1:c.626_627insGC ENSP00000516613.1:p.Lys210ProfsTer5
ENST00000706903.1:c.626_627insGC ENSP00000516614.1:p.Lys210ProfsTer5
ENST00000706904.1:c.626_627insGC ENSP00000516615.1:p.Lys210ProfsTer5
ENST00000706905.1:c.626_627insGC ENSP00000516616.1:p.Lys210ProfsTer5
ENST00000376809.10:c.626_627insGC MANE Select ENSP00000366005.5:p.Lys210ProfsTer5
ENST00000638375.1:c.626_627insGC ENSP00000492789.1:p.Lys210ProfsTer5
ENST00000376802.2:c.626_627insGC ENSP00000365998.2:p.Lys210ProfsTer5
ENST00000376806.9:c.626_627insGC ENSP00000366002.5:p.Lys210ProfsTer5
ENST00000376809.9:c.626_627insGC ENSP00000366005.5:p.Lys210ProfsTer5
ENST00000396634.5:c.626_627insGC ENSP00000379873.1:p.Lys210ProfsTer5
ENST00000461903.1:n.867_868insGC
ENST00000479320.5:n.867_868insGC
ENST00000495183.5:n.869_870insGC
ENST00000496081.5:n.443_444insGC
NM_002116.7:c.626_627insGC NP_002107.3:p.Lys210ProfsTer5
NM_002116.8:c.626_627insGC MANE Select NP_002107.3:p.Lys210ProfsTer5