Canonical Allele Identifier: CA2677796717

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945302-A-ATGTGTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945305_29945311dup , CM000668.2:g.29945305_29945311dup	GRCh38
NC_000006.11:g.29913082_29913088dup , CM000668.1:g.29913082_29913088dup	GRCh37
NC_000006.10:g.30021061_30021067dup	NCBI36
NG_029217.2:g.7841_7847dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.976+24_976+30dup	ENSP00000492789.2:n.976+24_976+30dup
ENST00000706892.1:n.2657_2663dup
ENST00000706893.1:c.*77+24_*77+30dup	ENSP00000516609.1:n.*77+24_*77+30dup
ENST00000706894.1:c.1117_1123dup	ENSP00000516610.1:p.Gly375ValfsTer30
ENST00000706895.1:n.1937_1943dup
ENST00000706896.1:n.2389+24_2389+30dup
ENST00000706897.1:n.1811+24_1811+30dup
ENST00000706898.1:c.1111+24_1111+30dup	ENSP00000516611.1:n.1111+24_1111+30dup
ENST00000706899.1:n.1947+24_1947+30dup
ENST00000706900.1:c.1009+24_1009+30dup	ENSP00000516617.1:n.1009+24_1009+30dup
ENST00000706901.1:c.1093+24_1093+30dup	ENSP00000516612.1:n.1093+24_1093+30dup
ENST00000706902.1:c.1093+24_1093+30dup	ENSP00000516613.1:n.1093+24_1093+30dup
ENST00000706903.1:c.1093+24_1093+30dup	ENSP00000516614.1:n.1093+24_1093+30dup
ENST00000706904.1:c.1093+24_1093+30dup	ENSP00000516615.1:n.1093+24_1093+30dup
ENST00000706905.1:c.1093+24_1093+30dup	ENSP00000516616.1:n.1093+24_1093+30dup
ENST00000376809.10:c.1093+24_1093+30dup MANE Select	ENSP00000366005.5:n.1093+24_1093+30dup
ENST00000376802.2:c.896-146_896-140dup	ENSP00000365998.2:n.896-146_896-140dup
ENST00000376806.9:c.1111+24_1111+30dup	ENSP00000366002.5:n.1111+24_1111+30dup
ENST00000376809.9:c.1093+24_1093+30dup	ENSP00000366005.5:n.1093+24_1093+30dup
ENST00000396634.5:c.1093+24_1093+30dup	ENSP00000379873.1:n.1093+24_1093+30dup
ENST00000495183.5:n.1332+24_1332+30dup
ENST00000496081.5:n.1352+24_1352+30dup
NM_002116.7:c.1093+24_1093+30dup	NP_002107.3:n.1093+24_1093+30dup
NM_002116.8:c.1093+24_1093+30dup MANE Select	NP_002107.3:n.1093+24_1093+30dup