Canonical Allele Identifier: CA363289651

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29942799-C-G
• MyVariant Identifiers: chr6:g.29910576C>G (hg19) ; chr6:g.29942799C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942799C>G , CM000668.2:g.29942799C>G	GRCh38
NC_000006.11:g.29910576C>G , CM000668.1:g.29910576C>G	GRCh37
NC_000006.10:g.30018555C>G	NCBI36
NG_029217.2:g.5334C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.116C>G	ENSP00000492789.2:p.Pro39Arg
ENST00000706892.1:n.392C>G
ENST00000706893.1:c.116C>G	ENSP00000516609.1:p.Pro39Arg
ENST00000706894.1:c.116C>G	ENSP00000516610.1:p.Pro39Arg
ENST00000706895.1:n.392C>G
ENST00000706896.1:n.392C>G
ENST00000706897.1:n.392C>G
ENST00000706898.1:c.116C>G	ENSP00000516611.1:p.Pro39Arg
ENST00000706899.1:n.392C>G
ENST00000706900.1:c.32C>G	ENSP00000516617.1:p.Pro11Arg
ENST00000706901.1:c.116C>G	ENSP00000516612.1:p.Pro39Arg
ENST00000706902.1:c.116C>G	ENSP00000516613.1:p.Pro39Arg
ENST00000706903.1:c.116C>G	ENSP00000516614.1:p.Pro39Arg
ENST00000706904.1:c.116C>G	ENSP00000516615.1:p.Pro39Arg
ENST00000706905.1:c.116C>G	ENSP00000516616.1:p.Pro39Arg
ENST00000376809.10:c.116C>G MANE Select	ENSP00000366005.5:p.Pro39Arg
ENST00000638375.1:c.116C>G	ENSP00000492789.1:p.Pro39Arg
ENST00000376802.2:c.116C>G	ENSP00000365998.2:p.Pro39Arg
ENST00000376806.9:c.116C>G	ENSP00000366002.5:p.Pro39Arg
ENST00000376809.9:c.116C>G	ENSP00000366005.5:p.Pro39Arg
ENST00000396634.5:c.116C>G	ENSP00000379873.1:p.Pro39Arg
ENST00000429656.1:n.269G>C
ENST00000461903.1:n.116C>G
ENST00000479320.5:n.116C>G
ENST00000495183.5:n.118C>G
ENST00000496081.5:n.122C>G
NM_002116.7:c.116C>G	NP_002107.3:p.Pro39Arg
NM_002116.8:c.116C>G MANE Select	NP_002107.3:p.Pro39Arg