Canonical Allele Identifier: CA1618520878
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945566C= , CM000668.2:g.29945566C= GRCh38
NC_000006.11:g.29913343C= , CM000668.1:g.29913343C= GRCh37
NC_000006.10:g.30021322C= NCBI36
NG_029217.2:g.8102C=

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.1092C= ENSP00000492789.2:n.1092C=
ENST00000706892.1:n.2918C=
ENST00000706893.1:c.*193C= ENSP00000516609.1:n.*193C=
ENST00000706894.1:c.*193C= ENSP00000516610.1:n.*193C=
ENST00000706895.1:n.2198C=
ENST00000706896.1:n.2505C=
ENST00000706897.1:n.1927C=
ENST00000706898.1:c.*111C= ENSP00000516611.1:n.*111C=
ENST00000706899.1:n.2063C=
ENST00000706900.1:c.*111C= ENSP00000516617.1:n.*111C=
ENST00000706901.1:c.*111C= ENSP00000516612.1:n.*111C=
ENST00000706902.1:c.1093+285C= ENSP00000516613.1:n.1093+285C=
ENST00000706903.1:c.*111C= ENSP00000516614.1:n.*111C=
ENST00000706904.1:c.1093+285C= ENSP00000516615.1:n.1093+285C=
ENST00000706905.1:c.*111C= ENSP00000516616.1:n.*111C=
ENST00000376809.10:c.*111C= MANE Select ENSP00000366005.5:n.*111C=
ENST00000376802.2:c.*111C= ENSP00000365998.2:n.*111C=
ENST00000376806.9:c.*111C= ENSP00000366002.5:n.*111C=
ENST00000376809.9:c.*111C= ENSP00000366005.5:n.*111C=
ENST00000396634.5:c.*111C= ENSP00000379873.1:n.*111C=
ENST00000495183.5:n.1448C=
ENST00000496081.5:n.1468C=
NM_002116.7:c.*111C= NP_002107.3:n.*111C=
NM_002116.8:c.*111C= MANE Select NP_002107.3:n.*111C=