Canonical Allele Identifier: CA2677798031

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945640-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945640C>A , CM000668.2:g.29945640C>A	GRCh38
NC_000006.11:g.29913417C>A , CM000668.1:g.29913417C>A	GRCh37
NC_000006.10:g.30021396C>A	NCBI36
NG_029217.2:g.8176C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.1166C>A	ENSP00000492789.2:n.1166C>A
ENST00000706892.1:n.2992C>A
ENST00000706893.1:c.*267C>A	ENSP00000516609.1:n.*267C>A
ENST00000706894.1:c.*267C>A	ENSP00000516610.1:n.*267C>A
ENST00000706895.1:n.2272C>A
ENST00000706896.1:n.2579C>A
ENST00000706897.1:n.2001C>A
ENST00000706898.1:c.*185C>A	ENSP00000516611.1:n.*185C>A
ENST00000706899.1:n.2137C>A
ENST00000706900.1:c.*185C>A	ENSP00000516617.1:n.*185C>A
ENST00000706901.1:c.*185C>A	ENSP00000516612.1:n.*185C>A
ENST00000706902.1:c.1093+359C>A	ENSP00000516613.1:n.1093+359C>A
ENST00000706903.1:c.*124+61C>A	ENSP00000516614.1:n.*124+61C>A
ENST00000706904.1:c.1093+359C>A	ENSP00000516615.1:n.1093+359C>A
ENST00000706905.1:c.*185C>A	ENSP00000516616.1:n.*185C>A
ENST00000376809.10:c.*185C>A MANE Select	ENSP00000366005.5:n.*185C>A
ENST00000376802.2:c.*185C>A	ENSP00000365998.2:n.*185C>A
ENST00000376806.9:c.*185C>A	ENSP00000366002.5:n.*185C>A
ENST00000376809.9:c.*185C>A	ENSP00000366005.5:n.*185C>A
ENST00000396634.5:c.*185C>A	ENSP00000379873.1:n.*185C>A
ENST00000495183.5:n.1522C>A
ENST00000496081.5:n.1542C>A
NM_002116.7:c.*185C>A	NP_002107.3:n.*185C>A
NM_002116.8:c.*185C>A MANE Select	NP_002107.3:n.*185C>A