Canonical Allele Identifier: CA2677951229

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271109-ATCTGCGGAGCCACTCCACGCACG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271111_31271133del , CM000668.2:g.31271111_31271133del	GRCh38
NC_000006.11:g.31238888_31238910del , CM000668.1:g.31238888_31238910del	GRCh37
NC_000006.10:g.31346867_31346889del	NCBI36
NG_029422.2:g.6000_6022del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.560_582del MANE Select	ENSP00000365402.5:p.Thr187IlefsTer26
ENST00000376228.9:c.560_582del	ENSP00000365402.5:p.Thr187IlefsTer26
ENST00000376237.8:c.*147_*169del	ENSP00000365412.4:n.*147_*169del
ENST00000383329.7:c.560_582del	ENSP00000372819.3:p.Thr187IlefsTer26
ENST00000415537.1:c.558_580del
ENST00000484378.1:n.829_851del
ENST00000487245.5:n.919_941del
ENST00000495835.1:n.749_771del
NM_002117.5:c.560_582del	NP_002108.4:p.Thr187IlefsTer26
NM_002117.6:c.560_582del MANE Select	NP_002108.4:p.Thr187IlefsTer26