Canonical Allele Identifier: CA136025999

Gene: HLA-A

Linked Data

• dbSNP Id: rs573809399
• gnomAD v2: 6-29913588-G-C
• gnomAD v3: 6-29945811-G-C
• gnomAD v4: 6-29945811-G-C
• MyVariant Identifiers: chr6:g.29913588G>C (hg19) ; chr6:g.29945811G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945811G>C , CM000668.2:g.29945811G>C	GRCh38
NC_000006.11:g.29913588G>C , CM000668.1:g.29913588G>C	GRCh37
NC_000006.10:g.30021567G>C	NCBI36
NG_029217.2:g.8347G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1337G>C	ENSP00000492789.2:n.1337G>C
ENST00000706896.1:n.2750G>C
ENST00000706897.1:n.2172G>C
ENST00000706898.1:c.*356G>C	ENSP00000516611.1:n.*356G>C
ENST00000706899.1:n.2308G>C
ENST00000706900.1:c.*356G>C	ENSP00000516617.1:n.*356G>C
ENST00000706901.1:c.*356G>C	ENSP00000516612.1:n.*356G>C
ENST00000706902.1:c.1093+530G>C	ENSP00000516613.1:n.1093+530G>C
ENST00000706903.1:c.*124+232G>C	ENSP00000516614.1:n.*124+232G>C
ENST00000706904.1:c.1093+530G>C	ENSP00000516615.1:n.1093+530G>C
ENST00000706905.1:c.*356G>C	ENSP00000516616.1:n.*356G>C
ENST00000376809.10:c.*356G>C MANE Select	ENSP00000366005.5:n.*356G>C
ENST00000376802.2:c.*356G>C	ENSP00000365998.2:n.*356G>C
ENST00000376806.9:c.*356G>C	ENSP00000366002.5:n.*356G>C
ENST00000376809.9:c.*356G>C	ENSP00000366005.5:n.*356G>C
ENST00000396634.5:c.*356G>C	ENSP00000379873.1:n.*356G>C
ENST00000495183.5:n.1693G>C
ENST00000496081.5:n.1713G>C
NM_002116.7:c.*356G>C	NP_002107.3:n.*356G>C
NM_002116.8:c.*356G>C MANE Select	NP_002107.3:n.*356G>C