Canonical Allele Identifier: CA136023334
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs199474519
gnomAD v4: 6-29943368-C-A
MyVariant Identifiers: chr6:g.29911145C>A (hg19) chr6:g.29943368C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943368C>A , CM000668.2:g.29943368C>A GRCh38
NC_000006.11:g.29911145C>A , CM000668.1:g.29911145C>A GRCh37
NC_000006.10:g.30019124C>A NCBI36
NG_029217.2:g.5903C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.444C>A ENSP00000492789.2:p.Ile148=
ENST00000706892.1:n.720C>A
ENST00000706893.1:c.444C>A ENSP00000516609.1:p.Ile148=
ENST00000706894.1:c.444C>A ENSP00000516610.1:p.Ile148=
ENST00000706895.1:n.720C>A
ENST00000706896.1:n.720C>A
ENST00000706897.1:n.720C>A
ENST00000706898.1:c.444C>A ENSP00000516611.1:p.Ile148=
ENST00000706899.1:n.720C>A
ENST00000706900.1:c.360C>A ENSP00000516617.1:p.Ile120=
ENST00000706901.1:c.444C>A ENSP00000516612.1:p.Ile148=
ENST00000706902.1:c.444C>A ENSP00000516613.1:p.Ile148=
ENST00000706903.1:c.444C>A ENSP00000516614.1:p.Ile148=
ENST00000706904.1:c.444C>A ENSP00000516615.1:p.Ile148=
ENST00000706905.1:c.444C>A ENSP00000516616.1:p.Ile148=
ENST00000376809.10:c.444C>A MANE Select ENSP00000366005.5:p.Ile148=
ENST00000638375.1:c.444C>A ENSP00000492789.1:p.Ile148=
ENST00000376802.2:c.444C>A ENSP00000365998.2:p.Ile148=
ENST00000376806.9:c.444C>A ENSP00000366002.5:p.Ile148=
ENST00000376809.9:c.444C>A ENSP00000366005.5:p.Ile148=
ENST00000396634.5:c.444C>A ENSP00000379873.1:p.Ile148=
ENST00000461903.1:n.685C>A
ENST00000479320.5:n.685C>A
ENST00000495183.5:n.687C>A
ENST00000496081.5:n.261C>A
NM_002116.7:c.444C>A NP_002107.3:p.Ile148=
NM_002116.8:c.444C>A MANE Select NP_002107.3:p.Ile148=
Search 100 bp 5'
Search 100 bp 3'