Canonical Allele Identifier: CA2677798062

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945651-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945655del , CM000668.2:g.29945655del	GRCh38
NC_000006.11:g.29913432del , CM000668.1:g.29913432del	GRCh37
NC_000006.10:g.30021411del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.1181del	ENSP00000492789.2:n.1181del
ENST00000706892.1:n.3007del
ENST00000706893.1:c.*282del	ENSP00000516609.1:n.*282del
ENST00000706894.1:c.*282del	ENSP00000516610.1:n.*282del
ENST00000706895.1:n.2287del
ENST00000706896.1:n.2594del
ENST00000706897.1:n.2016del
ENST00000706898.1:c.*200del	ENSP00000516611.1:n.*200del
ENST00000706899.1:n.2152del
ENST00000706900.1:c.*200del	ENSP00000516617.1:n.*200del
ENST00000706901.1:c.*200del	ENSP00000516612.1:n.*200del
ENST00000706902.1:c.1093+374del	ENSP00000516613.1:n.1093+374del
ENST00000706903.1:c.*124+76del	ENSP00000516614.1:n.*124+76del
ENST00000706904.1:c.1093+374del	ENSP00000516615.1:n.1093+374del
ENST00000706905.1:c.*200del	ENSP00000516616.1:n.*200del
ENST00000376809.10:c.*200del MANE Select	ENSP00000366005.5:n.*200del
ENST00000376802.2:c.*200del	ENSP00000365998.2:n.*200del
ENST00000376806.9:c.*200del	ENSP00000366002.5:n.*200del
ENST00000376809.9:c.*200del	ENSP00000366005.5:n.*200del
ENST00000396634.5:c.*200del	ENSP00000379873.1:n.*200del
ENST00000495183.5:n.1537del
ENST00000496081.5:n.1557del
NM_002116.7:c.*200del	NP_002107.3:n.*200del
NM_002116.8:c.*200del MANE Select	NP_002107.3:n.*200del