Canonical Allele Identifier: CA478845464
Gene: CDKN1B HGNC NCBI

Linked Data

COSMIC: COSM392360
MyVariant Identifiers: chr12:g.12870878del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717945del , CM000674.2:g.12717945del GRCh38
NC_000012.11:g.12870879del , CM000674.1:g.12870879del GRCh37
NC_000012.10:g.12762146del NCBI36
NG_016341.1:g.5578del

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.106del ENSP00000507272.1:p.Val36TrpfsTer6
ENST00000682620.1:n.1631-880del
ENST00000684771.1:n.585-880del
ENST00000228872.9:c.106del MANE Select ENSP00000228872.4:p.Val36TrpfsTer6
ENST00000228872.8:c.106del ENSP00000228872.4:p.Val36TrpfsTer6
ENST00000396340.1:c.106del ENSP00000379629.1:p.Val36TrpfsTer6
ENST00000442489.1:c.85del ENSP00000407597.1:p.Val29TrpfsTer6
ENST00000477087.1:n.155-880del
NM_004064.4:c.106del NP_004055.1:p.Val36TrpfsTer6
NM_004064.5:c.106del MANE Select NP_004055.1:p.Val36TrpfsTer6