Canonical Allele Identifier: CA2677797345

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945437-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945444dup , CM000668.2:g.29945444dup	GRCh38
NC_000006.11:g.29913221dup , CM000668.1:g.29913221dup	GRCh37
NC_000006.10:g.30021200dup	NCBI36
NG_029217.2:g.7980dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.977-7dup	ENSP00000492789.2:n.977-7dup
ENST00000706892.1:n.2796dup
ENST00000706893.1:c.*78-7dup	ENSP00000516609.1:n.*78-7dup
ENST00000706894.1:c.*71dup	ENSP00000516610.1:n.*71dup
ENST00000706895.1:n.2076dup
ENST00000706896.1:n.2390-7dup
ENST00000706897.1:n.1812-7dup
ENST00000706898.1:c.1112-7dup	ENSP00000516611.1:n.1112-7dup
ENST00000706899.1:n.1948-7dup
ENST00000706900.1:c.1010-7dup	ENSP00000516617.1:n.1010-7dup
ENST00000706901.1:c.1094-7dup	ENSP00000516612.1:n.1094-7dup
ENST00000706902.1:c.1093+163dup	ENSP00000516613.1:n.1093+163dup
ENST00000706903.1:c.1094-7dup	ENSP00000516614.1:n.1094-7dup
ENST00000706904.1:c.1093+163dup	ENSP00000516615.1:n.1093+163dup
ENST00000706905.1:c.1094-7dup	ENSP00000516616.1:n.1094-7dup
ENST00000376809.10:c.1094-7dup MANE Select	ENSP00000366005.5:n.1094-7dup
ENST00000376802.2:c.896-7dup	ENSP00000365998.2:n.896-7dup
ENST00000376806.9:c.1112-7dup	ENSP00000366002.5:n.1112-7dup
ENST00000376809.9:c.1094-7dup	ENSP00000366005.5:n.1094-7dup
ENST00000396634.5:c.1094-7dup	ENSP00000379873.1:n.1094-7dup
ENST00000495183.5:n.1333-7dup
ENST00000496081.5:n.1353-7dup
NM_002116.7:c.1094-7dup	NP_002107.3:n.1094-7dup
NM_002116.8:c.1094-7dup MANE Select	NP_002107.3:n.1094-7dup