Canonical Allele Identifier: CA2677951557
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271497_31271502del , CM000668.2:g.31271497_31271502del GRCh38
NC_000006.11:g.31239274_31239279del , CM000668.1:g.31239274_31239279del GRCh37
NC_000006.10:g.31347253_31347258del NCBI36
NG_029422.2:g.5630_5635del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.343+97_343+102del MANE Select ENSP00000365402.5:n.343+97_343+102del
ENST00000376228.9:c.343+97_343+102del ENSP00000365402.5:n.343+97_343+102del
ENST00000376237.8:c.343+97_343+102del ENSP00000365412.4:n.343+97_343+102del
ENST00000383329.7:c.343+97_343+102del ENSP00000372819.3:n.343+97_343+102del
ENST00000415537.1:c.341+97_341+102del
ENST00000484378.1:n.459_464del
ENST00000487245.5:n.549_554del
ENST00000495835.1:n.532+97_532+102del
NM_002117.5:c.343+97_343+102del NP_002108.4:n.343+97_343+102del
NM_002117.6:c.343+97_343+102del MANE Select NP_002108.4:n.343+97_343+102del