Canonical Allele Identifier: CA2677797594

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945508-TTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945511_29945512del , CM000668.2:g.29945511_29945512del	GRCh38
NC_000006.11:g.29913288_29913289del , CM000668.1:g.29913288_29913289del	GRCh37
NC_000006.10:g.30021267_30021268del	NCBI36
NG_029217.2:g.8047_8048del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1037_1038del	ENSP00000492789.2:n.1037_1038del
ENST00000706892.1:n.2863_2864del
ENST00000706893.1:c.*138_*139del	ENSP00000516609.1:n.*138_*139del
ENST00000706894.1:c.*138_*139del	ENSP00000516610.1:n.*138_*139del
ENST00000706895.1:n.2143_2144del
ENST00000706896.1:n.2450_2451del
ENST00000706897.1:n.1872_1873del
ENST00000706898.1:c.*56_*57del	ENSP00000516611.1:n.*56_*57del
ENST00000706899.1:n.2008_2009del
ENST00000706900.1:c.*56_*57del	ENSP00000516617.1:n.*56_*57del
ENST00000706901.1:c.*56_*57del	ENSP00000516612.1:n.*56_*57del
ENST00000706902.1:c.1093+230_1093+231del	ENSP00000516613.1:n.1093+230_1093+231del
ENST00000706903.1:c.*56_*57del	ENSP00000516614.1:n.*56_*57del
ENST00000706904.1:c.1093+230_1093+231del	ENSP00000516615.1:n.1093+230_1093+231del
ENST00000706905.1:c.*56_*57del	ENSP00000516616.1:n.*56_*57del
ENST00000376809.10:c.*56_*57del MANE Select	ENSP00000366005.5:n.*56_*57del
ENST00000376802.2:c.*56_*57del	ENSP00000365998.2:n.*56_*57del
ENST00000376806.9:c.*56_*57del	ENSP00000366002.5:n.*56_*57del
ENST00000376809.9:c.*56_*57del	ENSP00000366005.5:n.*56_*57del
ENST00000396634.5:c.*56_*57del	ENSP00000379873.1:n.*56_*57del
ENST00000495183.5:n.1393_1394del
ENST00000496081.5:n.1413_1414del
NM_002116.7:c.*56_*57del	NP_002107.3:n.*56_*57del
NM_002116.8:c.*56_*57del MANE Select	NP_002107.3:n.*56_*57del