Canonical Allele Identifier: CA363047886

Gene: HLA-A

Linked Data

• gnomAD v3: 6-29944550-G-T
• gnomAD v4: 6-29944550-G-T
• MyVariant Identifiers: chr6:g.29912327G>T (hg19) ; chr6:g.29944550G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944550G>T , CM000668.2:g.29944550G>T	GRCh38
NC_000006.11:g.29912327G>T , CM000668.1:g.29912327G>T	GRCh37
NC_000006.10:g.30020306G>T	NCBI36
NG_029217.2:g.7086G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+153G>T	ENSP00000492789.2:n.895+153G>T
ENST00000706892.1:n.1902G>T
ENST00000706893.1:c.980G>T	ENSP00000516609.1:p.Gly327Val
ENST00000706894.1:c.946G>T	ENSP00000516610.1:p.Val316Phe
ENST00000706895.1:n.1324G>T
ENST00000706896.1:n.1800G>T
ENST00000706897.1:n.1222G>T
ENST00000706898.1:c.946G>T	ENSP00000516611.1:p.Val316Phe
ENST00000706899.1:n.1800G>T
ENST00000706900.1:c.862G>T	ENSP00000516617.1:p.Val288Phe
ENST00000706901.1:c.946G>T	ENSP00000516612.1:p.Val316Phe
ENST00000706902.1:c.946G>T	ENSP00000516613.1:p.Val316Phe
ENST00000706903.1:c.946G>T	ENSP00000516614.1:p.Val316Phe
ENST00000706904.1:c.946G>T	ENSP00000516615.1:p.Val316Phe
ENST00000706905.1:c.946G>T	ENSP00000516616.1:p.Val316Phe
ENST00000376809.10:c.946G>T MANE Select	ENSP00000366005.5:p.Val316Phe
ENST00000638375.1:c.895+153G>T	ENSP00000492789.1:n.895+153G>T
ENST00000376802.2:c.895+153G>T	ENSP00000365998.2:n.895+153G>T
ENST00000376806.9:c.946G>T	ENSP00000366002.5:p.Val316Phe
ENST00000376809.9:c.946G>T	ENSP00000366005.5:p.Val316Phe
ENST00000396634.5:c.946G>T	ENSP00000379873.1:p.Val316Phe
ENST00000461903.1:n.1187G>T
ENST00000479320.5:n.1187G>T
ENST00000495183.5:n.1189G>T
ENST00000496081.5:n.763G>T
NM_002116.7:c.946G>T	NP_002107.3:p.Val316Phe
NM_002116.8:c.946G>T MANE Select	NP_002107.3:p.Val316Phe