Canonical Allele Identifier: CA2677951298

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271195-ATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271197_31271198del , CM000668.2:g.31271197_31271198del	GRCh38
NC_000006.11:g.31238974_31238975del , CM000668.1:g.31238974_31238975del	GRCh37
NC_000006.10:g.31346953_31346954del	NCBI36
NG_029422.2:g.5935_5936del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.495_496del MANE Select	ENSP00000365402.5:p.Gln165HisfsTer?
ENST00000376228.9:c.495_496del	ENSP00000365402.5:p.Gln165HisfsTer?
ENST00000376237.8:c.*82_*83del	ENSP00000365412.4:n.*82_*83del
ENST00000383329.7:c.495_496del	ENSP00000372819.3:p.Gln165HisfsTer?
ENST00000415537.1:c.493_494del
ENST00000484378.1:n.764_765del
ENST00000487245.5:n.854_855del
ENST00000495835.1:n.684_685del
NM_002117.5:c.495_496del	NP_002108.4:p.Gln165HisfsTer?
NM_002117.6:c.495_496del MANE Select	NP_002108.4:p.Gln165HisfsTer?