Canonical Allele Identifier: CA3693776

Gene: HLA-A

Linked Data

• dbSNP Id: rs572407231
• ExAC: 6:29913274 T / C
• gnomAD v2: 6-29913274-T-C
• gnomAD v3: 6-29945497-T-C
• gnomAD v4: 6-29945497-T-C
• MyVariant Identifiers: chr6:g.29913274T>C (hg19) ; chr6:g.29945497T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945497T>C , CM000668.2:g.29945497T>C	GRCh38
NC_000006.11:g.29913274T>C , CM000668.1:g.29913274T>C	GRCh37
NC_000006.10:g.30021253T>C	NCBI36
NG_029217.2:g.8033T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1023T>C	ENSP00000492789.2:n.1023T>C
ENST00000706892.1:n.2849T>C
ENST00000706893.1:c.*124T>C	ENSP00000516609.1:n.*124T>C
ENST00000706894.1:c.*124T>C	ENSP00000516610.1:n.*124T>C
ENST00000706895.1:n.2129T>C
ENST00000706896.1:n.2436T>C
ENST00000706897.1:n.1858T>C
ENST00000706898.1:c.*42T>C	ENSP00000516611.1:n.*42T>C
ENST00000706899.1:n.1994T>C
ENST00000706900.1:c.*42T>C	ENSP00000516617.1:n.*42T>C
ENST00000706901.1:c.*42T>C	ENSP00000516612.1:n.*42T>C
ENST00000706902.1:c.1093+216T>C	ENSP00000516613.1:n.1093+216T>C
ENST00000706903.1:c.*42T>C	ENSP00000516614.1:n.*42T>C
ENST00000706904.1:c.1093+216T>C	ENSP00000516615.1:n.1093+216T>C
ENST00000706905.1:c.*42T>C	ENSP00000516616.1:n.*42T>C
ENST00000376809.10:c.*42T>C MANE Select	ENSP00000366005.5:n.*42T>C
ENST00000376802.2:c.*42T>C	ENSP00000365998.2:n.*42T>C
ENST00000376806.9:c.*42T>C	ENSP00000366002.5:n.*42T>C
ENST00000376809.9:c.*42T>C	ENSP00000366005.5:n.*42T>C
ENST00000396634.5:c.*42T>C	ENSP00000379873.1:n.*42T>C
ENST00000495183.5:n.1379T>C
ENST00000496081.5:n.1399T>C
NM_002116.7:c.*42T>C	NP_002107.3:n.*42T>C
NM_002116.8:c.*42T>C MANE Select	NP_002107.3:n.*42T>C