Canonical Allele Identifier: CA2677950672
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270355del , CM000668.2:g.31270355del GRCh38
NC_000006.11:g.31238132del , CM000668.1:g.31238132del GRCh37
NC_000006.10:g.31346111del NCBI36
NG_029422.2:g.6778del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.751del MANE Select ENSP00000365402.5:p.Asp251ThrfsTer?
ENST00000376228.9:c.751del ENSP00000365402.5:p.Asp251ThrfsTer?
ENST00000376237.8:c.*338del ENSP00000365412.4:n.*338del
ENST00000383329.7:c.751del ENSP00000372819.3:p.Asp251ThrfsTer?
ENST00000415537.1:c.665-23del
ENST00000470363.5:n.69del
ENST00000487245.5:n.1110del
ENST00000495835.1:n.940del
NM_002117.5:c.751del NP_002108.4:p.Asp251ThrfsTer?
NM_002117.6:c.751del MANE Select NP_002108.4:p.Asp251ThrfsTer?