Canonical Allele Identifier: CA823769926

Gene: HLA-A

Linked Data

• dbSNP Id: rs1332278838
• gnomAD v3: 6-29945656-AATC-A
• gnomAD v4: 6-29945656-AATC-A
• MyVariant Identifiers: chr6:g.29913434_29913436del (hg19) ; chr6:g.29945657_29945659del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945660_29945662del , CM000668.2:g.29945660_29945662del	GRCh38
NC_000006.11:g.29913437_29913439del , CM000668.1:g.29913437_29913439del	GRCh37
NC_000006.10:g.30021416_30021418del	NCBI36
NG_029217.2:g.8196_8198del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1186_1188del	ENSP00000492789.2:n.1186_1188del
ENST00000706892.1:n.3012_3014del
ENST00000706893.1:c.*287_*289del	ENSP00000516609.1:n.*287_*289del
ENST00000706894.1:c.*287_*289del	ENSP00000516610.1:n.*287_*289del
ENST00000706895.1:n.2292_2294del
ENST00000706896.1:n.2599_2601del
ENST00000706897.1:n.2021_2023del
ENST00000706898.1:c.*205_*207del	ENSP00000516611.1:n.*205_*207del
ENST00000706899.1:n.2157_2159del
ENST00000706900.1:c.*205_*207del	ENSP00000516617.1:n.*205_*207del
ENST00000706901.1:c.*205_*207del	ENSP00000516612.1:n.*205_*207del
ENST00000706902.1:c.1093+379_1093+381del	ENSP00000516613.1:n.1093+379_1093+381del
ENST00000706903.1:c.*124+81_*124+83del	ENSP00000516614.1:n.*124+81_*124+83del
ENST00000706904.1:c.1093+379_1093+381del	ENSP00000516615.1:n.1093+379_1093+381del
ENST00000706905.1:c.*205_*207del	ENSP00000516616.1:n.*205_*207del
ENST00000376809.10:c.*205_*207del MANE Select	ENSP00000366005.5:n.*205_*207del
ENST00000376802.2:c.*205_*207del	ENSP00000365998.2:n.*205_*207del
ENST00000376806.9:c.*205_*207del	ENSP00000366002.5:n.*205_*207del
ENST00000376809.9:c.*205_*207del	ENSP00000366005.5:n.*205_*207del
ENST00000396634.5:c.*205_*207del	ENSP00000379873.1:n.*205_*207del
ENST00000495183.5:n.1542_1544del
ENST00000496081.5:n.1562_1564del
NM_002116.7:c.*205_*207del	NP_002107.3:n.*205_*207del
NM_002116.8:c.*205_*207del MANE Select	NP_002107.3:n.*205_*207del