Canonical Allele Identifier: CA2677796246

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29943337-GGCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29943339_29943341del , CM000668.2:g.29943339_29943341del	GRCh38
NC_000006.11:g.29911116_29911118del , CM000668.1:g.29911116_29911118del	GRCh37
NC_000006.10:g.30019095_30019097del	NCBI36
NG_029217.2:g.5874_5876del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.415_417del	ENSP00000492789.2:p.Gln139del
ENST00000706892.1:n.691_693del
ENST00000706893.1:c.415_417del	ENSP00000516609.1:p.Gln139del
ENST00000706894.1:c.415_417del	ENSP00000516610.1:p.Gln139del
ENST00000706895.1:n.691_693del
ENST00000706896.1:n.691_693del
ENST00000706897.1:n.691_693del
ENST00000706898.1:c.415_417del	ENSP00000516611.1:p.Gln139del
ENST00000706899.1:n.691_693del
ENST00000706900.1:c.331_333del	ENSP00000516617.1:p.Gln111del
ENST00000706901.1:c.415_417del	ENSP00000516612.1:p.Gln139del
ENST00000706902.1:c.415_417del	ENSP00000516613.1:p.Gln139del
ENST00000706903.1:c.415_417del	ENSP00000516614.1:p.Gln139del
ENST00000706904.1:c.415_417del	ENSP00000516615.1:p.Gln139del
ENST00000706905.1:c.415_417del	ENSP00000516616.1:p.Gln139del
ENST00000376809.10:c.415_417del MANE Select	ENSP00000366005.5:p.Gln139del
ENST00000638375.1:c.415_417del	ENSP00000492789.1:p.Gln139del
ENST00000376802.2:c.415_417del	ENSP00000365998.2:p.Gln139del
ENST00000376806.9:c.415_417del	ENSP00000366002.5:p.Gln139del
ENST00000376809.9:c.415_417del	ENSP00000366005.5:p.Gln139del
ENST00000396634.5:c.415_417del	ENSP00000379873.1:p.Gln139del
ENST00000461903.1:n.656_658del
ENST00000479320.5:n.656_658del
ENST00000495183.5:n.658_660del
ENST00000496081.5:n.232_234del
NM_002116.7:c.415_417del	NP_002107.3:p.Gln139del
NM_002116.8:c.415_417del MANE Select	NP_002107.3:p.Gln139del