Canonical Allele Identifier: CA2677949103
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268908_31268909insCG , CM000668.2:g.31268908_31268909insCG GRCh38
NC_000006.11:g.31236685_31236686insCG , CM000668.1:g.31236685_31236686insCG GRCh37
NC_000006.10:g.31344664_31344665insCG NCBI36
NG_029422.2:g.8223_8224insCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*260_*261insCG MANE Select ENSP00000365402.5:n.*260_*261insCG
ENST00000376228.9:c.*260_*261insCG ENSP00000365402.5:n.*260_*261insCG
ENST00000376237.8:c.*948_*949insCG ENSP00000365412.4:n.*948_*949insCG
ENST00000383329.7:c.*260_*261insCG ENSP00000372819.3:n.*260_*261insCG
ENST00000466892.5:n.594_595insCG
ENST00000470363.5:n.1119_1120insCG
ENST00000487245.5:n.1720_1721insCG
NM_002117.5:c.*260_*261insCG NP_002108.4:n.*260_*261insCG
NM_002117.6:c.*260_*261insCG MANE Select NP_002108.4:n.*260_*261insCG