Canonical Allele Identifier: CA2677949773

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269475-CCCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269481_31269483del , CM000668.2:g.31269481_31269483del	GRCh38
NC_000006.11:g.31237258_31237260del , CM000668.1:g.31237258_31237260del	GRCh37
NC_000006.10:g.31345237_31345239del	NCBI36
NG_029422.2:g.7654_7656del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048+15_1048+17del MANE Select	ENSP00000365402.5:n.1048+15_1048+17del
ENST00000376228.9:c.1048+15_1048+17del	ENSP00000365402.5:n.1048+15_1048+17del
ENST00000376237.8:c.*635+15_*635+17del	ENSP00000365412.4:n.*635+15_*635+17del
ENST00000383329.7:c.1066+15_1066+17del	ENSP00000372819.3:n.1066+15_1066+17del
ENST00000466892.5:n.189_191del
ENST00000470363.5:n.806+15_806+17del
ENST00000487245.5:n.1407+15_1407+17del
NM_002117.5:c.1048+15_1048+17del	NP_002108.4:n.1048+15_1048+17del
NM_002117.6:c.1048+15_1048+17del MANE Select	NP_002108.4:n.1048+15_1048+17del