Canonical Allele Identifier: CA2581558128

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945862-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945862A>T , CM000668.2:g.29945862A>T	GRCh38
NC_000006.11:g.29913639A>T , CM000668.1:g.29913639A>T	GRCh37
NC_000006.10:g.30021618A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1388A>T	ENSP00000492789.2:n.1388A>T
ENST00000706900.1:c.*407A>T	ENSP00000516617.1:n.*407A>T
ENST00000706901.1:c.*407A>T	ENSP00000516612.1:n.*407A>T
ENST00000706902.1:c.1093+581A>T	ENSP00000516613.1:n.1093+581A>T
ENST00000706903.1:c.*124+283A>T	ENSP00000516614.1:n.*124+283A>T
ENST00000706904.1:c.1093+581A>T	ENSP00000516615.1:n.1093+581A>T
ENST00000706905.1:c.*407A>T	ENSP00000516616.1:n.*407A>T
ENST00000376809.10:c.*407A>T MANE Select	ENSP00000366005.5:n.*407A>T
ENST00000376802.2:c.*407A>T	ENSP00000365998.2:n.*407A>T
ENST00000376806.9:c.*407A>T	ENSP00000366002.5:n.*407A>T
ENST00000376809.9:c.*407A>T	ENSP00000366005.5:n.*407A>T
ENST00000396634.5:c.*407A>T	ENSP00000379873.1:n.*407A>T
ENST00000495183.5:n.1744A>T
ENST00000496081.5:n.1764A>T
NM_002116.7:c.*407A>T	NP_002107.3:n.*407A>T
NM_002116.8:c.*407A>T MANE Select	NP_002107.3:n.*407A>T