Canonical Allele Identifier: CA2677951410
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271378_31271379insT , CM000668.2:g.31271378_31271379insT GRCh38
NC_000006.11:g.31239155_31239156insT , CM000668.1:g.31239155_31239156insT GRCh37
NC_000006.10:g.31347134_31347135insT NCBI36
NG_029422.2:g.5753_5754insA

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.344-31_344-30insA MANE Select ENSP00000365402.5:n.344-31_344-30insA
ENST00000376228.9:c.344-31_344-30insA ENSP00000365402.5:n.344-31_344-30insA
ENST00000376237.8:c.344-48_344-47insA ENSP00000365412.4:n.344-48_344-47insA
ENST00000383329.7:c.344-31_344-30insA ENSP00000372819.3:n.344-31_344-30insA
ENST00000415537.1:c.342-31_342-30insA
ENST00000484378.1:n.582_583insA
ENST00000487245.5:n.672_673insA
ENST00000495835.1:n.533-31_533-30insA
NM_002117.5:c.344-31_344-30insA NP_002108.4:n.344-31_344-30insA
NM_002117.6:c.344-31_344-30insA MANE Select NP_002108.4:n.344-31_344-30insA