Canonical Allele Identifier: CA2677951351
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271330del , CM000668.2:g.31271330del GRCh38
NC_000006.11:g.31239107del , CM000668.1:g.31239107del GRCh37
NC_000006.10:g.31347086del NCBI36
NG_029422.2:g.5803del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.363del MANE Select ENSP00000365402.5:p.Met122CysfsTer29
ENST00000376228.9:c.363del ENSP00000365402.5:p.Met122CysfsTer29
ENST00000376237.8:c.346del ENSP00000365412.4:p.Asp116MetfsTer?
ENST00000383329.7:c.363del ENSP00000372819.3:p.Met122CysfsTer29
ENST00000415537.1:c.361del
ENST00000484378.1:n.632del
ENST00000487245.5:n.722del
ENST00000495835.1:n.552del
NM_002117.5:c.363del NP_002108.4:p.Met122CysfsTer29
NM_002117.6:c.363del MANE Select NP_002108.4:p.Met122CysfsTer29