Canonical Allele Identifier: CA650546359

Gene: HLA-A

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945576_29945577insC , CM000668.2:g.29945576_29945577insC	GRCh38
NC_000006.11:g.29913353_29913354insC , CM000668.1:g.29913353_29913354insC	GRCh37
NC_000006.10:g.30021332_30021333insC	NCBI36
NG_029217.2:g.8112_8113insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1102_1103insC	ENSP00000492789.2:n.1102_1103insC
ENST00000706892.1:n.2928_2929insC
ENST00000706893.1:c.*203_*204insC	ENSP00000516609.1:n.*203_*204insC
ENST00000706894.1:c.*203_*204insC	ENSP00000516610.1:n.*203_*204insC
ENST00000706895.1:n.2208_2209insC
ENST00000706896.1:n.2515_2516insC
ENST00000706897.1:n.1937_1938insC
ENST00000706898.1:c.*121_*122insC	ENSP00000516611.1:n.*121_*122insC
ENST00000706899.1:n.2073_2074insC
ENST00000706900.1:c.*121_*122insC	ENSP00000516617.1:n.*121_*122insC
ENST00000706901.1:c.*121_*122insC	ENSP00000516612.1:n.*121_*122insC
ENST00000706902.1:c.1093+295_1093+296insC	ENSP00000516613.1:n.1093+295_1093+296insC
ENST00000706903.1:c.*121_*122insC	ENSP00000516614.1:n.*121_*122insC
ENST00000706904.1:c.1093+295_1093+296insC	ENSP00000516615.1:n.1093+295_1093+296insC
ENST00000706905.1:c.*121_*122insC	ENSP00000516616.1:n.*121_*122insC
ENST00000376809.10:c.*121_*122insC MANE Select	ENSP00000366005.5:n.*121_*122insC
ENST00000376802.2:c.*121_*122insC	ENSP00000365998.2:n.*121_*122insC
ENST00000376806.9:c.*121_*122insC	ENSP00000366002.5:n.*121_*122insC
ENST00000376809.9:c.*121_*122insC	ENSP00000366005.5:n.*121_*122insC
ENST00000396634.5:c.*121_*122insC	ENSP00000379873.1:n.*121_*122insC
ENST00000495183.5:n.1458_1459insC
ENST00000496081.5:n.1478_1479insC
NM_002116.7:c.*121_*122insC	NP_002107.3:n.*121_*122insC
NM_002116.8:c.*121_*122insC MANE Select	NP_002107.3:n.*121_*122insC