Canonical Allele Identifier: CA136026016

Gene: HLA-A

Linked Data

• dbSNP Id: rs1554116722
• gnomAD v4: 6-29945861-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945862del , CM000668.2:g.29945862del	GRCh38
NC_000006.11:g.29913639del , CM000668.1:g.29913639del	GRCh37
NC_000006.10:g.30021618del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1388del	ENSP00000492789.2:n.1388del
ENST00000706900.1:c.*407del	ENSP00000516617.1:n.*407del
ENST00000706901.1:c.*407del	ENSP00000516612.1:n.*407del
ENST00000706902.1:c.1093+581del	ENSP00000516613.1:n.1093+581del
ENST00000706903.1:c.*124+283del	ENSP00000516614.1:n.*124+283del
ENST00000706904.1:c.1093+581del	ENSP00000516615.1:n.1093+581del
ENST00000706905.1:c.*407del	ENSP00000516616.1:n.*407del
ENST00000376809.10:c.*407del MANE Select	ENSP00000366005.5:n.*407del
ENST00000376802.2:c.*407del	ENSP00000365998.2:n.*407del
ENST00000376806.9:c.*407del	ENSP00000366002.5:n.*407del
ENST00000376809.9:c.*407del	ENSP00000366005.5:n.*407del
ENST00000396634.5:c.*407del	ENSP00000379873.1:n.*407del
ENST00000495183.5:n.1744del
ENST00000496081.5:n.1764del
NM_002116.7:c.*407del	NP_002107.3:n.*407del
NM_002116.8:c.*407del MANE Select	NP_002107.3:n.*407del