Canonical Allele Identifier: CA136023551

Gene: HLA-A

Linked Data

• dbSNP Id: rs79442106
• gnomAD v3: 6-29943410-G-A
• gnomAD v4: 6-29943410-G-A
• MyVariant Identifiers: chr6:g.29911187G>A (hg19) ; chr6:g.29943410G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29943410G>A , CM000668.2:g.29943410G>A	GRCh38
NC_000006.11:g.29911187G>A , CM000668.1:g.29911187G>A	GRCh37
NC_000006.10:g.30019166G>A	NCBI36
NG_029217.2:g.5945G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.486G>A	ENSP00000492789.2:p.Met162Ile
ENST00000706892.1:n.762G>A
ENST00000706893.1:c.486G>A	ENSP00000516609.1:p.Met162Ile
ENST00000706894.1:c.486G>A	ENSP00000516610.1:p.Met162Ile
ENST00000706895.1:n.762G>A
ENST00000706896.1:n.762G>A
ENST00000706897.1:n.762G>A
ENST00000706898.1:c.486G>A	ENSP00000516611.1:p.Met162Ile
ENST00000706899.1:n.762G>A
ENST00000706900.1:c.402G>A	ENSP00000516617.1:p.Met134Ile
ENST00000706901.1:c.486G>A	ENSP00000516612.1:p.Met162Ile
ENST00000706902.1:c.486G>A	ENSP00000516613.1:p.Met162Ile
ENST00000706903.1:c.486G>A	ENSP00000516614.1:p.Met162Ile
ENST00000706904.1:c.486G>A	ENSP00000516615.1:p.Met162Ile
ENST00000706905.1:c.486G>A	ENSP00000516616.1:p.Met162Ile
ENST00000376809.10:c.486G>A MANE Select	ENSP00000366005.5:p.Met162Ile
ENST00000638375.1:c.486G>A	ENSP00000492789.1:p.Met162Ile
ENST00000376802.2:c.486G>A	ENSP00000365998.2:p.Met162Ile
ENST00000376806.9:c.486G>A	ENSP00000366002.5:p.Met162Ile
ENST00000376809.9:c.486G>A	ENSP00000366005.5:p.Met162Ile
ENST00000396634.5:c.486G>A	ENSP00000379873.1:p.Met162Ile
ENST00000461903.1:n.727G>A
ENST00000479320.5:n.727G>A
ENST00000495183.5:n.729G>A
ENST00000496081.5:n.303G>A
NM_002116.7:c.486G>A	NP_002107.3:p.Met162Ile
NM_002116.8:c.486G>A MANE Select	NP_002107.3:p.Met162Ile