Canonical Allele Identifier: CA136024684
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs199474619

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944218T>G , CM000668.2:g.29944218T>G GRCh38
NC_000006.11:g.29911995T>G , CM000668.1:g.29911995T>G GRCh37
NC_000006.10:g.30019974T>G NCBI36
NG_029217.2:g.6754T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.716T>G ENSP00000492789.2:p.Leu239Arg
ENST00000706892.1:n.1570T>G
ENST00000706893.1:c.716T>G ENSP00000516609.1:p.Leu239Arg
ENST00000706894.1:c.716T>G ENSP00000516610.1:p.Leu239Arg
ENST00000706895.1:n.992T>G
ENST00000706896.1:n.1570T>G
ENST00000706897.1:n.992T>G
ENST00000706898.1:c.716T>G ENSP00000516611.1:p.Leu239Arg
ENST00000706899.1:n.1570T>G
ENST00000706900.1:c.632T>G ENSP00000516617.1:p.Leu211Arg
ENST00000706901.1:c.716T>G ENSP00000516612.1:p.Leu239Arg
ENST00000706902.1:c.716T>G ENSP00000516613.1:p.Leu239Arg
ENST00000706903.1:c.716T>G ENSP00000516614.1:p.Leu239Arg
ENST00000706904.1:c.716T>G ENSP00000516615.1:p.Leu239Arg
ENST00000706905.1:c.716T>G ENSP00000516616.1:p.Leu239Arg
ENST00000376809.10:c.716T>G MANE Select ENSP00000366005.5:p.Leu239Arg
ENST00000638375.1:c.716T>G ENSP00000492789.1:p.Leu239Arg
ENST00000376802.2:c.716T>G ENSP00000365998.2:p.Leu239Arg
ENST00000376806.9:c.716T>G ENSP00000366002.5:p.Leu239Arg
ENST00000376809.9:c.716T>G ENSP00000366005.5:p.Leu239Arg
ENST00000396634.5:c.716T>G ENSP00000379873.1:p.Leu239Arg
ENST00000461903.1:n.957T>G
ENST00000479320.5:n.957T>G
ENST00000495183.5:n.959T>G
ENST00000496081.5:n.533T>G
NM_002116.7:c.716T>G NP_002107.3:p.Leu239Arg
NM_002116.8:c.716T>G MANE Select NP_002107.3:p.Leu239Arg