Canonical Allele Identifier: CA363048621

Gene: HLA-A

Linked Data

• dbSNP Id: rs369261720
• gnomAD v2: 6-29913020-G-C
• gnomAD v4: 6-29945243-G-C
• MyVariant Identifiers: chr6:g.29913020G>C (hg19) ; chr6:g.29945243G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945243G>C , CM000668.2:g.29945243G>C	GRCh38
NC_000006.11:g.29913020G>C , CM000668.1:g.29913020G>C	GRCh37
NC_000006.10:g.30020999G>C	NCBI36
NG_029217.2:g.7779G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.938G>C	ENSP00000492789.2:p.Ser313Thr
ENST00000706892.1:n.2595G>C
ENST00000706893.1:c.*39G>C	ENSP00000516609.1:n.*39G>C
ENST00000706894.1:c.1055G>C	ENSP00000516610.1:p.Ser352Thr
ENST00000706895.1:n.1875G>C
ENST00000706896.1:n.2351G>C
ENST00000706897.1:n.1773G>C
ENST00000706898.1:c.1073G>C	ENSP00000516611.1:p.Ser358Thr
ENST00000706899.1:n.1909G>C
ENST00000706900.1:c.971G>C	ENSP00000516617.1:p.Ser324Thr
ENST00000706901.1:c.1055G>C	ENSP00000516612.1:p.Ser352Thr
ENST00000706902.1:c.1055G>C	ENSP00000516613.1:p.Ser352Thr
ENST00000706903.1:c.1055G>C	ENSP00000516614.1:p.Ser352Thr
ENST00000706904.1:c.1055G>C	ENSP00000516615.1:p.Ser352Thr
ENST00000706905.1:c.1055G>C	ENSP00000516616.1:p.Ser352Thr
ENST00000376809.10:c.1055G>C MANE Select	ENSP00000366005.5:p.Ser352Thr
ENST00000638375.1:c.938G>C	ENSP00000492789.1:p.Ser313Thr
ENST00000376802.2:c.896-208G>C	ENSP00000365998.2:n.896-208G>C
ENST00000376806.9:c.1073G>C	ENSP00000366002.5:p.Ser358Thr
ENST00000376809.9:c.1055G>C	ENSP00000366005.5:p.Ser352Thr
ENST00000396634.5:c.1055G>C	ENSP00000379873.1:p.Ser352Thr
ENST00000461903.1:n.1314G>C
ENST00000479320.5:n.1296G>C
ENST00000495183.5:n.1294G>C
ENST00000496081.5:n.1314G>C
NM_002116.7:c.1055G>C	NP_002107.3:p.Ser352Thr
NM_002116.8:c.1055G>C MANE Select	NP_002107.3:p.Ser352Thr