Canonical Allele Identifier: CA2677950651

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31270316-TCCATCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270318_31270324del , CM000668.2:g.31270318_31270324del	GRCh38
NC_000006.11:g.31238095_31238101del , CM000668.1:g.31238095_31238101del	GRCh37
NC_000006.10:g.31346074_31346080del	NCBI36
NG_029422.2:g.6809_6815del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.782_788del MANE Select	ENSP00000365402.5:p.Gly261GlufsTer?
ENST00000376228.9:c.782_788del	ENSP00000365402.5:p.Gly261GlufsTer?
ENST00000376237.8:c.*369_*375del	ENSP00000365412.4:n.*369_*375del
ENST00000383329.7:c.782_788del	ENSP00000372819.3:p.Gly261GlufsTer?
ENST00000415537.1:c.673_679del
ENST00000470363.5:n.100_106del
ENST00000487245.5:n.1141_1147del
ENST00000495835.1:n.971_977del
NM_002117.5:c.782_788del	NP_002108.4:p.Gly261GlufsTer?
NM_002117.6:c.782_788del MANE Select	NP_002108.4:p.Gly261GlufsTer?