Canonical Allele Identifier: CA650546362

Gene: HLA-A

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945578_29945579insG , CM000668.2:g.29945578_29945579insG	GRCh38
NC_000006.11:g.29913355_29913356insG , CM000668.1:g.29913355_29913356insG	GRCh37
NC_000006.10:g.30021334_30021335insG	NCBI36
NG_029217.2:g.8114_8115insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1104_1105insG	ENSP00000492789.2:n.1104_1105insG
ENST00000706892.1:n.2930_2931insG
ENST00000706893.1:c.*205_*206insG	ENSP00000516609.1:n.*205_*206insG
ENST00000706894.1:c.*205_*206insG	ENSP00000516610.1:n.*205_*206insG
ENST00000706895.1:n.2210_2211insG
ENST00000706896.1:n.2517_2518insG
ENST00000706897.1:n.1939_1940insG
ENST00000706898.1:c.*123_*124insG	ENSP00000516611.1:n.*123_*124insG
ENST00000706899.1:n.2075_2076insG
ENST00000706900.1:c.*123_*124insG	ENSP00000516617.1:n.*123_*124insG
ENST00000706901.1:c.*123_*124insG	ENSP00000516612.1:n.*123_*124insG
ENST00000706902.1:c.1093+297_1093+298insG	ENSP00000516613.1:n.1093+297_1093+298insG
ENST00000706903.1:c.*123_*124insG	ENSP00000516614.1:n.*123_*124insG
ENST00000706904.1:c.1093+297_1093+298insG	ENSP00000516615.1:n.1093+297_1093+298insG
ENST00000706905.1:c.*123_*124insG	ENSP00000516616.1:n.*123_*124insG
ENST00000376809.10:c.*123_*124insG MANE Select	ENSP00000366005.5:n.*123_*124insG
ENST00000376802.2:c.*123_*124insG	ENSP00000365998.2:n.*123_*124insG
ENST00000376806.9:c.*123_*124insG	ENSP00000366002.5:n.*123_*124insG
ENST00000376809.9:c.*123_*124insG	ENSP00000366005.5:n.*123_*124insG
ENST00000396634.5:c.*123_*124insG	ENSP00000379873.1:n.*123_*124insG
ENST00000495183.5:n.1460_1461insG
ENST00000496081.5:n.1480_1481insG
NM_002116.7:c.*123_*124insG	NP_002107.3:n.*123_*124insG
NM_002116.8:c.*123_*124insG MANE Select	NP_002107.3:n.*123_*124insG