Canonical Allele Identifier: CA2677949195
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268968_31268969insCT , CM000668.2:g.31268968_31268969insCT GRCh38
NC_000006.11:g.31236745_31236746insCT , CM000668.1:g.31236745_31236746insCT GRCh37
NC_000006.10:g.31344724_31344725insCT NCBI36
NG_029422.2:g.8163_8164insAG

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*200_*201insAG MANE Select ENSP00000365402.5:n.*200_*201insAG
ENST00000376228.9:c.*200_*201insAG ENSP00000365402.5:n.*200_*201insAG
ENST00000376237.8:c.*888_*889insAG ENSP00000365412.4:n.*888_*889insAG
ENST00000383329.7:c.*200_*201insAG ENSP00000372819.3:n.*200_*201insAG
ENST00000466892.5:n.534_535insAG
ENST00000470363.5:n.1059_1060insAG
ENST00000487245.5:n.1660_1661insAG
NM_002117.5:c.*200_*201insAG NP_002108.4:n.*200_*201insAG
NM_002117.6:c.*200_*201insAG MANE Select NP_002108.4:n.*200_*201insAG