Canonical Allele Identifier: CA2677951402
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271375_31271376insC , CM000668.2:g.31271375_31271376insC GRCh38
NC_000006.11:g.31239152_31239153insC , CM000668.1:g.31239152_31239153insC GRCh37
NC_000006.10:g.31347131_31347132insC NCBI36
NG_029422.2:g.5756_5757insG

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.344-28_344-27insG MANE Select ENSP00000365402.5:n.344-28_344-27insG
ENST00000376228.9:c.344-28_344-27insG ENSP00000365402.5:n.344-28_344-27insG
ENST00000376237.8:c.344-45_344-44insG ENSP00000365412.4:n.344-45_344-44insG
ENST00000383329.7:c.344-28_344-27insG ENSP00000372819.3:n.344-28_344-27insG
ENST00000415537.1:c.342-28_342-27insG
ENST00000484378.1:n.585_586insG
ENST00000487245.5:n.675_676insG
ENST00000495835.1:n.533-28_533-27insG
NM_002117.5:c.344-28_344-27insG NP_002108.4:n.344-28_344-27insG
NM_002117.6:c.344-28_344-27insG MANE Select NP_002108.4:n.344-28_344-27insG