Canonical Allele Identifier: CA2677951426
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271392_31271393insG , CM000668.2:g.31271392_31271393insG GRCh38
NC_000006.11:g.31239169_31239170insG , CM000668.1:g.31239169_31239170insG GRCh37
NC_000006.10:g.31347148_31347149insG NCBI36
NG_029422.2:g.5739_5740insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-45_344-44insC MANE Select ENSP00000365402.5:n.344-45_344-44insC
ENST00000376228.9:c.344-45_344-44insC ENSP00000365402.5:n.344-45_344-44insC
ENST00000376237.8:c.344-62_344-61insC ENSP00000365412.4:n.344-62_344-61insC
ENST00000383329.7:c.344-45_344-44insC ENSP00000372819.3:n.344-45_344-44insC
ENST00000415537.1:c.342-45_342-44insC
ENST00000484378.1:n.568_569insC
ENST00000487245.5:n.658_659insC
ENST00000495835.1:n.533-45_533-44insC
NM_002117.5:c.344-45_344-44insC NP_002108.4:n.344-45_344-44insC
NM_002117.6:c.344-45_344-44insC MANE Select NP_002108.4:n.344-45_344-44insC