Canonical Allele Identifier: CA2677951637
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271560_31271565del , CM000668.2:g.31271560_31271565del GRCh38
NC_000006.11:g.31239337_31239342del , CM000668.1:g.31239337_31239342del GRCh37
NC_000006.10:g.31347316_31347321del NCBI36
NG_029422.2:g.5570_5575del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+37_343+42del MANE Select ENSP00000365402.5:n.343+37_343+42del
ENST00000376228.9:c.343+37_343+42del ENSP00000365402.5:n.343+37_343+42del
ENST00000376237.8:c.343+37_343+42del ENSP00000365412.4:n.343+37_343+42del
ENST00000383329.7:c.343+37_343+42del ENSP00000372819.3:n.343+37_343+42del
ENST00000415537.1:c.341+37_341+42del
ENST00000484378.1:n.399_404del
ENST00000487245.5:n.489_494del
ENST00000495835.1:n.532+37_532+42del
NM_002117.5:c.343+37_343+42del NP_002108.4:n.343+37_343+42del
NM_002117.6:c.343+37_343+42del MANE Select NP_002108.4:n.343+37_343+42del