Canonical Allele Identifier: CA363048769

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945283-T-A
• MyVariant Identifiers: chr6:g.29913060T>A (hg19) ; chr6:g.29945283T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945283T>A , CM000668.2:g.29945283T>A	GRCh38
NC_000006.11:g.29913060T>A , CM000668.1:g.29913060T>A	GRCh37
NC_000006.10:g.30021039T>A	NCBI36
NG_029217.2:g.7819T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.976+2T>A	ENSP00000492789.2:n.976+2T>A
ENST00000706892.1:n.2635T>A
ENST00000706893.1:c.*77+2T>A	ENSP00000516609.1:n.*77+2T>A
ENST00000706894.1:c.1095T>A	ENSP00000516610.1:p.Gly365=
ENST00000706895.1:n.1915T>A
ENST00000706896.1:n.2389+2T>A
ENST00000706897.1:n.1811+2T>A
ENST00000706898.1:c.1111+2T>A	ENSP00000516611.1:n.1111+2T>A
ENST00000706899.1:n.1947+2T>A
ENST00000706900.1:c.1009+2T>A	ENSP00000516617.1:n.1009+2T>A
ENST00000706901.1:c.1093+2T>A	ENSP00000516612.1:n.1093+2T>A
ENST00000706902.1:c.1093+2T>A	ENSP00000516613.1:n.1093+2T>A
ENST00000706903.1:c.1093+2T>A	ENSP00000516614.1:n.1093+2T>A
ENST00000706904.1:c.1093+2T>A	ENSP00000516615.1:n.1093+2T>A
ENST00000706905.1:c.1093+2T>A	ENSP00000516616.1:n.1093+2T>A
ENST00000376809.10:c.1093+2T>A MANE Select	ENSP00000366005.5:n.1093+2T>A
ENST00000376802.2:c.896-168T>A	ENSP00000365998.2:n.896-168T>A
ENST00000376806.9:c.1111+2T>A	ENSP00000366002.5:n.1111+2T>A
ENST00000376809.9:c.1093+2T>A	ENSP00000366005.5:n.1093+2T>A
ENST00000396634.5:c.1093+2T>A	ENSP00000379873.1:n.1093+2T>A
ENST00000495183.5:n.1332+2T>A
ENST00000496081.5:n.1352+2T>A
NM_002116.7:c.1093+2T>A	NP_002107.3:n.1093+2T>A
NM_002116.8:c.1093+2T>A MANE Select	NP_002107.3:n.1093+2T>A