Canonical Allele Identifier: CA2677798305

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945723-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945723A>C , CM000668.2:g.29945723A>C	GRCh38
NC_000006.11:g.29913500A>C , CM000668.1:g.29913500A>C	GRCh37
NC_000006.10:g.30021479A>C	NCBI36
NG_029217.2:g.8259A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1249A>C	ENSP00000492789.2:n.1249A>C
ENST00000706893.1:c.*350A>C	ENSP00000516609.1:n.*350A>C
ENST00000706894.1:c.*350A>C	ENSP00000516610.1:n.*350A>C
ENST00000706895.1:n.2355A>C
ENST00000706896.1:n.2662A>C
ENST00000706897.1:n.2084A>C
ENST00000706898.1:c.*268A>C	ENSP00000516611.1:n.*268A>C
ENST00000706899.1:n.2220A>C
ENST00000706900.1:c.*268A>C	ENSP00000516617.1:n.*268A>C
ENST00000706901.1:c.*268A>C	ENSP00000516612.1:n.*268A>C
ENST00000706902.1:c.1093+442A>C	ENSP00000516613.1:n.1093+442A>C
ENST00000706903.1:c.*124+144A>C	ENSP00000516614.1:n.*124+144A>C
ENST00000706904.1:c.1093+442A>C	ENSP00000516615.1:n.1093+442A>C
ENST00000706905.1:c.*268A>C	ENSP00000516616.1:n.*268A>C
ENST00000376809.10:c.*268A>C MANE Select	ENSP00000366005.5:n.*268A>C
ENST00000376802.2:c.*268A>C	ENSP00000365998.2:n.*268A>C
ENST00000376806.9:c.*268A>C	ENSP00000366002.5:n.*268A>C
ENST00000376809.9:c.*268A>C	ENSP00000366005.5:n.*268A>C
ENST00000396634.5:c.*268A>C	ENSP00000379873.1:n.*268A>C
ENST00000495183.5:n.1605A>C
ENST00000496081.5:n.1625A>C
NM_002116.7:c.*268A>C	NP_002107.3:n.*268A>C
NM_002116.8:c.*268A>C MANE Select	NP_002107.3:n.*268A>C