Canonical Allele Identifier: CA2677951167
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271038_31271039del , CM000668.2:g.31271038_31271039del GRCh38
NC_000006.11:g.31238815_31238816del , CM000668.1:g.31238815_31238816del GRCh37
NC_000006.10:g.31346794_31346795del NCBI36
NG_029422.2:g.6093_6094del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.619+34_619+35del MANE Select ENSP00000365402.5:n.619+34_619+35del
ENST00000376228.9:c.619+34_619+35del ENSP00000365402.5:n.619+34_619+35del
ENST00000376237.8:c.*206+34_*206+35del ENSP00000365412.4:n.*206+34_*206+35del
ENST00000383329.7:c.619+34_619+35del ENSP00000372819.3:n.619+34_619+35del
ENST00000415537.1:c.617+34_617+35del
ENST00000487245.5:n.978+34_978+35del
ENST00000495835.1:n.808+34_808+35del
NM_002117.5:c.619+34_619+35del NP_002108.4:n.619+34_619+35del
NM_002117.6:c.619+34_619+35del MANE Select NP_002108.4:n.619+34_619+35del