Canonical Allele Identifier: CA363048737

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945273-C-T
• MyVariant Identifiers: chr6:g.29913050C>T (hg19) ; chr6:g.29945273C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945273C>T , CM000668.2:g.29945273C>T	GRCh38
NC_000006.11:g.29913050C>T , CM000668.1:g.29913050C>T	GRCh37
NC_000006.10:g.30021029C>T	NCBI36
NG_029217.2:g.7809C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.968C>T	ENSP00000492789.2:p.Ala323Val
ENST00000706892.1:n.2625C>T
ENST00000706893.1:c.*69C>T	ENSP00000516609.1:n.*69C>T
ENST00000706894.1:c.1085C>T	ENSP00000516610.1:p.Ala362Val
ENST00000706895.1:n.1905C>T
ENST00000706896.1:n.2381C>T
ENST00000706897.1:n.1803C>T
ENST00000706898.1:c.1103C>T	ENSP00000516611.1:p.Ala368Val
ENST00000706899.1:n.1939C>T
ENST00000706900.1:c.1001C>T	ENSP00000516617.1:p.Ala334Val
ENST00000706901.1:c.1085C>T	ENSP00000516612.1:p.Ala362Val
ENST00000706902.1:c.1085C>T	ENSP00000516613.1:p.Ala362Val
ENST00000706903.1:c.1085C>T	ENSP00000516614.1:p.Ala362Val
ENST00000706904.1:c.1085C>T	ENSP00000516615.1:p.Ala362Val
ENST00000706905.1:c.1085C>T	ENSP00000516616.1:p.Ala362Val
ENST00000376809.10:c.1085C>T MANE Select	ENSP00000366005.5:p.Ala362Val
ENST00000638375.1:c.968C>T	ENSP00000492789.1:p.Ala323Val
ENST00000376802.2:c.896-178C>T	ENSP00000365998.2:n.896-178C>T
ENST00000376806.9:c.1103C>T	ENSP00000366002.5:p.Ala368Val
ENST00000376809.9:c.1085C>T	ENSP00000366005.5:p.Ala362Val
ENST00000396634.5:c.1085C>T	ENSP00000379873.1:p.Ala362Val
ENST00000461903.1:n.1344C>T
ENST00000479320.5:n.1326C>T
ENST00000495183.5:n.1324C>T
ENST00000496081.5:n.1344C>T
NM_002116.7:c.1085C>T	NP_002107.3:p.Ala362Val
NM_002116.8:c.1085C>T MANE Select	NP_002107.3:p.Ala362Val