Canonical Allele Identifier: CA2677797946

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945596-ACCACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945604_29945608del , CM000668.2:g.29945604_29945608del	GRCh38
NC_000006.11:g.29913381_29913385del , CM000668.1:g.29913381_29913385del	GRCh37
NC_000006.10:g.30021360_30021364del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1130_1134del	ENSP00000492789.2:n.1130_1134del
ENST00000706892.1:n.2956_2960del
ENST00000706893.1:c.*231_*235del	ENSP00000516609.1:n.*231_*235del
ENST00000706894.1:c.*231_*235del	ENSP00000516610.1:n.*231_*235del
ENST00000706895.1:n.2236_2240del
ENST00000706896.1:n.2543_2547del
ENST00000706897.1:n.1965_1969del
ENST00000706898.1:c.*149_*153del	ENSP00000516611.1:n.*149_*153del
ENST00000706899.1:n.2101_2105del
ENST00000706900.1:c.*149_*153del	ENSP00000516617.1:n.*149_*153del
ENST00000706901.1:c.*149_*153del	ENSP00000516612.1:n.*149_*153del
ENST00000706902.1:c.1093+323_1093+327del	ENSP00000516613.1:n.1093+323_1093+327del
ENST00000706903.1:c.*124+25_*124+29del	ENSP00000516614.1:n.*124+25_*124+29del
ENST00000706904.1:c.1093+323_1093+327del	ENSP00000516615.1:n.1093+323_1093+327del
ENST00000706905.1:c.*149_*153del	ENSP00000516616.1:n.*149_*153del
ENST00000376809.10:c.*149_*153del MANE Select	ENSP00000366005.5:n.*149_*153del
ENST00000376802.2:c.*149_*153del	ENSP00000365998.2:n.*149_*153del
ENST00000376806.9:c.*149_*153del	ENSP00000366002.5:n.*149_*153del
ENST00000376809.9:c.*149_*153del	ENSP00000366005.5:n.*149_*153del
ENST00000396634.5:c.*149_*153del	ENSP00000379873.1:n.*149_*153del
ENST00000495183.5:n.1486_1490del
ENST00000496081.5:n.1506_1510del
NM_002116.7:c.*149_*153del	NP_002107.3:n.*149_*153del
NM_002116.8:c.*149_*153del MANE Select	NP_002107.3:n.*149_*153del