Canonical Allele Identifier: CA1618519554
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944557_29944572delinsTTGGAGCTGTGATCAC , CM000668.2:g.29944557_29944572delinsTTGGAGCTGTGATCAC GRCh38
NC_000006.11:g.29912334_29912349delinsTTGGAGCTGTGATCAC , CM000668.1:g.29912334_29912349delinsTTGGAGCTGTGATCAC GRCh37
NC_000006.10:g.30020313_30020328delinsTTGGAGCTGTGATCAC NCBI36
NG_029217.2:g.7093_7108delinsTTGGAGCTGTGATCAC

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.895+160_895+175delinsTTGGAGCTGTGATCAC ENSP00000492789.2:n.895+160_895+175delins...
ENST00000706892.1:n.1909_1924delinsTTGGAGCTGTGATCAC
ENST00000706893.1:c.987_1002delinsTTGGAGCTGTGATCAC ENSP00000516609.1:p.Pro329=
ENST00000706894.1:c.953_968delinsTTGGAGCTGTGATCAC ENSP00000516610.1:p.Leu318=
ENST00000706895.1:n.1331_1346delinsTTGGAGCTGTGATCAC
ENST00000706896.1:n.1807_1822delinsTTGGAGCTGTGATCAC
ENST00000706897.1:n.1229_1244delinsTTGGAGCTGTGATCAC
ENST00000706898.1:c.953_968delinsTTGGAGCTGTGATCAC ENSP00000516611.1:p.Leu318=
ENST00000706899.1:n.1807_1822delinsTTGGAGCTGTGATCAC
ENST00000706900.1:c.869_884delinsTTGGAGCTGTGATCAC ENSP00000516617.1:p.Leu290=
ENST00000706901.1:c.953_968delinsTTGGAGCTGTGATCAC ENSP00000516612.1:p.Leu318=
ENST00000706902.1:c.953_968delinsTTGGAGCTGTGATCAC ENSP00000516613.1:p.Leu318=
ENST00000706903.1:c.953_968delinsTTGGAGCTGTGATCAC ENSP00000516614.1:p.Leu318=
ENST00000706904.1:c.953_968delinsTTGGAGCTGTGATCAC ENSP00000516615.1:p.Leu318=
ENST00000706905.1:c.953_968delinsTTGGAGCTGTGATCAC ENSP00000516616.1:p.Leu318=
ENST00000376809.10:c.953_968delinsTTGGAGCTGTGATCAC MANE Select ENSP00000366005.5:p.Leu318=
ENST00000638375.1:c.895+160_895+175delinsTTGGAGCTGTGATCAC ENSP00000492789.1:n.895+160_895+175delins...
ENST00000376802.2:c.895+160_895+175delinsTTGGAGCTGTGATCAC ENSP00000365998.2:n.895+160_895+175delins...
ENST00000376806.9:c.953_968delinsTTGGAGCTGTGATCAC ENSP00000366002.5:p.Leu318=
ENST00000376809.9:c.953_968delinsTTGGAGCTGTGATCAC ENSP00000366005.5:p.Leu318=
ENST00000396634.5:c.953_968delinsTTGGAGCTGTGATCAC ENSP00000379873.1:p.Leu318=
ENST00000461903.1:n.1194_1209delinsTTGGAGCTGTGATCAC
ENST00000479320.5:n.1194_1209delinsTTGGAGCTGTGATCAC
ENST00000495183.5:n.1196_1211delinsTTGGAGCTGTGATCAC
ENST00000496081.5:n.770_785delinsTTGGAGCTGTGATCAC
NM_002116.7:c.953_968delinsTTGGAGCTGTGATCAC NP_002107.3:p.Leu318=
NM_002116.8:c.953_968delinsTTGGAGCTGTGATCAC MANE Select NP_002107.3:p.Leu318=