Canonical Allele Identifier: CA136024966
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs281864770
gnomAD v4: 6-29944364-G-A
MyVariant Identifiers: chr6:g.29912141G>A (hg19) chr6:g.29944364G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944364G>A , CM000668.2:g.29944364G>A GRCh38
NC_000006.11:g.29912141G>A , CM000668.1:g.29912141G>A GRCh37
NC_000006.10:g.30020120G>A NCBI36
NG_029217.2:g.6900G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.862G>A ENSP00000492789.2:p.Glu288Lys
ENST00000706892.1:n.1716G>A
ENST00000706893.1:c.862G>A ENSP00000516609.1:p.Glu288Lys
ENST00000706894.1:c.862G>A ENSP00000516610.1:p.Glu288Lys
ENST00000706895.1:n.1138G>A
ENST00000706896.1:n.1716G>A
ENST00000706897.1:n.1138G>A
ENST00000706898.1:c.862G>A ENSP00000516611.1:p.Glu288Lys
ENST00000706899.1:n.1716G>A
ENST00000706900.1:c.778G>A ENSP00000516617.1:p.Glu260Lys
ENST00000706901.1:c.862G>A ENSP00000516612.1:p.Glu288Lys
ENST00000706902.1:c.862G>A ENSP00000516613.1:p.Glu288Lys
ENST00000706903.1:c.862G>A ENSP00000516614.1:p.Glu288Lys
ENST00000706904.1:c.862G>A ENSP00000516615.1:p.Glu288Lys
ENST00000706905.1:c.862G>A ENSP00000516616.1:p.Glu288Lys
ENST00000376809.10:c.862G>A MANE Select ENSP00000366005.5:p.Glu288Lys
ENST00000638375.1:c.862G>A ENSP00000492789.1:p.Glu288Lys
ENST00000376802.2:c.862G>A ENSP00000365998.2:p.Glu288Lys
ENST00000376806.9:c.862G>A ENSP00000366002.5:p.Glu288Lys
ENST00000376809.9:c.862G>A ENSP00000366005.5:p.Glu288Lys
ENST00000396634.5:c.862G>A ENSP00000379873.1:p.Glu288Lys
ENST00000461903.1:n.1103G>A
ENST00000479320.5:n.1103G>A
ENST00000495183.5:n.1105G>A
ENST00000496081.5:n.679G>A
NM_002116.7:c.862G>A NP_002107.3:p.Glu288Lys
NM_002116.8:c.862G>A MANE Select NP_002107.3:p.Glu288Lys
Search 100 bp 5'
Search 100 bp 3'