Canonical Allele Identifier: CA2677950618
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270184_31270187del , CM000668.2:g.31270184_31270187del GRCh38
NC_000006.11:g.31237961_31237964del , CM000668.1:g.31237961_31237964del GRCh37
NC_000006.10:g.31345940_31345943del NCBI36
NG_029422.2:g.6945_6948del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.895+23_895+26del MANE Select ENSP00000365402.5:n.895+23_895+26del
ENST00000376228.9:c.895+23_895+26del ENSP00000365402.5:n.895+23_895+26del
ENST00000376237.8:c.*482+23_*482+26del ENSP00000365412.4:n.*482+23_*482+26del
ENST00000383329.7:c.895+23_895+26del ENSP00000372819.3:n.895+23_895+26del
ENST00000470363.5:n.213+23_213+26del
ENST00000487245.5:n.1254+23_1254+26del
NM_002117.5:c.895+23_895+26del NP_002108.4:n.895+23_895+26del
NM_002117.6:c.895+23_895+26del MANE Select NP_002108.4:n.895+23_895+26del