Canonical Allele Identifier: CA2677798246
Gene: HLA-A HGNC NCBI

Linked Data

gnomAD v4: 6-29945710-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945710A>C , CM000668.2:g.29945710A>C GRCh38
NC_000006.11:g.29913487A>C , CM000668.1:g.29913487A>C GRCh37
NC_000006.10:g.30021466A>C NCBI36
NG_029217.2:g.8246A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.1236A>C ENSP00000492789.2:n.1236A>C
ENST00000706893.1:c.*337A>C ENSP00000516609.1:n.*337A>C
ENST00000706894.1:c.*337A>C ENSP00000516610.1:n.*337A>C
ENST00000706895.1:n.2342A>C
ENST00000706896.1:n.2649A>C
ENST00000706897.1:n.2071A>C
ENST00000706898.1:c.*255A>C ENSP00000516611.1:n.*255A>C
ENST00000706899.1:n.2207A>C
ENST00000706900.1:c.*255A>C ENSP00000516617.1:n.*255A>C
ENST00000706901.1:c.*255A>C ENSP00000516612.1:n.*255A>C
ENST00000706902.1:c.1093+429A>C ENSP00000516613.1:n.1093+429A>C
ENST00000706903.1:c.*124+131A>C ENSP00000516614.1:n.*124+131A>C
ENST00000706904.1:c.1093+429A>C ENSP00000516615.1:n.1093+429A>C
ENST00000706905.1:c.*255A>C ENSP00000516616.1:n.*255A>C
ENST00000376809.10:c.*255A>C MANE Select ENSP00000366005.5:n.*255A>C
ENST00000376802.2:c.*255A>C ENSP00000365998.2:n.*255A>C
ENST00000376806.9:c.*255A>C ENSP00000366002.5:n.*255A>C
ENST00000376809.9:c.*255A>C ENSP00000366005.5:n.*255A>C
ENST00000396634.5:c.*255A>C ENSP00000379873.1:n.*255A>C
ENST00000495183.5:n.1592A>C
ENST00000496081.5:n.1612A>C
NM_002116.7:c.*255A>C NP_002107.3:n.*255A>C
NM_002116.8:c.*255A>C MANE Select NP_002107.3:n.*255A>C