Canonical Allele Identifier: CA2677950486
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270121_31270122del , CM000668.2:g.31270121_31270122del GRCh38
NC_000006.11:g.31237898_31237899del , CM000668.1:g.31237898_31237899del GRCh37
NC_000006.10:g.31345877_31345878del NCBI36
NG_029422.2:g.7013_7014del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.896-34_896-33del MANE Select ENSP00000365402.5:n.896-34_896-33del
ENST00000376228.9:c.896-34_896-33del ENSP00000365402.5:n.896-34_896-33del
ENST00000376237.8:c.*483-34_*483-33del ENSP00000365412.4:n.*483-34_*483-33del
ENST00000383329.7:c.896-34_896-33del ENSP00000372819.3:n.896-34_896-33del
ENST00000470363.5:n.214-34_214-33del
ENST00000487245.5:n.1255-34_1255-33del
NM_002117.5:c.896-34_896-33del NP_002108.4:n.896-34_896-33del
NM_002117.6:c.896-34_896-33del MANE Select NP_002108.4:n.896-34_896-33del