Canonical Allele Identifier: CA2677951430
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271393_31271394insAGTCCCA , CM000668.2:g.31271393_31271394insAGTCCCA GRCh38
NC_000006.11:g.31239170_31239171insAGTCCCA , CM000668.1:g.31239170_31239171insAGTCCCA GRCh37
NC_000006.10:g.31347149_31347150insAGTCCCA NCBI36
NG_029422.2:g.5738_5739insTGGGACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-46_344-45insTGGGACT MANE Select ENSP00000365402.5:n.344-46_344-45insTGGGACT
ENST00000376228.9:c.344-46_344-45insTGGGACT ENSP00000365402.5:n.344-46_344-45insTGGGACT
ENST00000376237.8:c.344-63_344-62insTGGGACT ENSP00000365412.4:n.344-63_344-62insTGGGACT
ENST00000383329.7:c.344-46_344-45insTGGGACT ENSP00000372819.3:n.344-46_344-45insTGGGACT
ENST00000415537.1:c.342-46_342-45insTGGGACT
ENST00000484378.1:n.567_568insTGGGACT
ENST00000487245.5:n.657_658insTGGGACT
ENST00000495835.1:n.533-46_533-45insTGGGACT
NM_002117.5:c.344-46_344-45insTGGGACT NP_002108.4:n.344-46_344-45insTGGGACT
NM_002117.6:c.344-46_344-45insTGGGACT MANE Select NP_002108.4:n.344-46_344-45insTGGGACT