Canonical Allele Identifier: CA2578557170
Gene: HLA-A HGNC NCBI

Linked Data

gnomAD v4: 6-29945545-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945545G>A , CM000668.2:g.29945545G>A GRCh38
NC_000006.11:g.29913322G>A , CM000668.1:g.29913322G>A GRCh37
NC_000006.10:g.30021301G>A NCBI36
NG_029217.2:g.8081G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.1071G>A ENSP00000492789.2:n.1071G>A
ENST00000706892.1:n.2897G>A
ENST00000706893.1:c.*172G>A ENSP00000516609.1:n.*172G>A
ENST00000706894.1:c.*172G>A ENSP00000516610.1:n.*172G>A
ENST00000706895.1:n.2177G>A
ENST00000706896.1:n.2484G>A
ENST00000706897.1:n.1906G>A
ENST00000706898.1:c.*90G>A ENSP00000516611.1:n.*90G>A
ENST00000706899.1:n.2042G>A
ENST00000706900.1:c.*90G>A ENSP00000516617.1:n.*90G>A
ENST00000706901.1:c.*90G>A ENSP00000516612.1:n.*90G>A
ENST00000706902.1:c.1093+264G>A ENSP00000516613.1:n.1093+264G>A
ENST00000706903.1:c.*90G>A ENSP00000516614.1:n.*90G>A
ENST00000706904.1:c.1093+264G>A ENSP00000516615.1:n.1093+264G>A
ENST00000706905.1:c.*90G>A ENSP00000516616.1:n.*90G>A
ENST00000376809.10:c.*90G>A MANE Select ENSP00000366005.5:n.*90G>A
ENST00000376802.2:c.*90G>A ENSP00000365998.2:n.*90G>A
ENST00000376806.9:c.*90G>A ENSP00000366002.5:n.*90G>A
ENST00000376809.9:c.*90G>A ENSP00000366005.5:n.*90G>A
ENST00000396634.5:c.*90G>A ENSP00000379873.1:n.*90G>A
ENST00000495183.5:n.1427G>A
ENST00000496081.5:n.1447G>A
NM_002116.7:c.*90G>A NP_002107.3:n.*90G>A
NM_002116.8:c.*90G>A MANE Select NP_002107.3:n.*90G>A