Canonical Allele Identifier: CA2677951644
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271561del , CM000668.2:g.31271561del GRCh38
NC_000006.11:g.31239338del , CM000668.1:g.31239338del GRCh37
NC_000006.10:g.31347317del NCBI36
NG_029422.2:g.5571del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.343+38del MANE Select ENSP00000365402.5:n.343+38del
ENST00000376228.9:c.343+38del ENSP00000365402.5:n.343+38del
ENST00000376237.8:c.343+38del ENSP00000365412.4:n.343+38del
ENST00000383329.7:c.343+38del ENSP00000372819.3:n.343+38del
ENST00000415537.1:c.341+38del
ENST00000484378.1:n.400del
ENST00000487245.5:n.490del
ENST00000495835.1:n.532+38del
NM_002117.5:c.343+38del NP_002108.4:n.343+38del
NM_002117.6:c.343+38del MANE Select NP_002108.4:n.343+38del