Canonical Allele Identifier: CA449461411
Gene: HLA-A HGNC NCBI

Linked Data

gnomAD v4: 6-29944555-C-G
MyVariant Identifiers: chr6:g.29912332C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944555C>G , CM000668.2:g.29944555C>G GRCh38
NC_000006.11:g.29912332C>G , CM000668.1:g.29912332C>G GRCh37
NC_000006.10:g.30020311C>G NCBI36
NG_029217.2:g.7091C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.895+158C>G ENSP00000492789.2:n.895+158C>G
ENST00000706892.1:n.1907C>G
ENST00000706893.1:c.985C>G ENSP00000516609.1:p.Pro329Ala
ENST00000706894.1:c.951C>G ENSP00000516610.1:p.Leu317=
ENST00000706895.1:n.1329C>G
ENST00000706896.1:n.1805C>G
ENST00000706897.1:n.1227C>G
ENST00000706898.1:c.951C>G ENSP00000516611.1:p.Leu317=
ENST00000706899.1:n.1805C>G
ENST00000706900.1:c.867C>G ENSP00000516617.1:p.Leu289=
ENST00000706901.1:c.951C>G ENSP00000516612.1:p.Leu317=
ENST00000706902.1:c.951C>G ENSP00000516613.1:p.Leu317=
ENST00000706903.1:c.951C>G ENSP00000516614.1:p.Leu317=
ENST00000706904.1:c.951C>G ENSP00000516615.1:p.Leu317=
ENST00000706905.1:c.951C>G ENSP00000516616.1:p.Leu317=
ENST00000376809.10:c.951C>G MANE Select ENSP00000366005.5:p.Leu317=
ENST00000638375.1:c.895+158C>G ENSP00000492789.1:n.895+158C>G
ENST00000376802.2:c.895+158C>G ENSP00000365998.2:n.895+158C>G
ENST00000376806.9:c.951C>G ENSP00000366002.5:p.Leu317=
ENST00000376809.9:c.951C>G ENSP00000366005.5:p.Leu317=
ENST00000396634.5:c.951C>G ENSP00000379873.1:p.Leu317=
ENST00000461903.1:n.1192C>G
ENST00000479320.5:n.1192C>G
ENST00000495183.5:n.1194C>G
ENST00000496081.5:n.768C>G
NM_002116.7:c.951C>G NP_002107.3:p.Leu317=
NM_002116.8:c.951C>G MANE Select NP_002107.3:p.Leu317=