Canonical Allele Identifier: CA2677950717
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270464del , CM000668.2:g.31270464del GRCh38
NC_000006.11:g.31238241del , CM000668.1:g.31238241del GRCh37
NC_000006.10:g.31346220del NCBI36
NG_029422.2:g.6670del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.643del MANE Select ENSP00000365402.5:p.His215ThrfsTer11
ENST00000376228.9:c.643del ENSP00000365402.5:p.His215ThrfsTer11
ENST00000376237.8:c.*230del ENSP00000365412.4:n.*230del
ENST00000383329.7:c.643del ENSP00000372819.3:p.His215ThrfsTer11
ENST00000415537.1:c.641del
ENST00000487245.5:n.1002del
ENST00000495835.1:n.832del
NM_002117.5:c.643del NP_002108.4:p.His215ThrfsTer11
NM_002117.6:c.643del MANE Select NP_002108.4:p.His215ThrfsTer11