Canonical Allele Identifier: CA478845991
Gene: CDKN1B HGNC NCBI

Linked Data

COSMIC: COSM242497
MyVariant Identifiers: chr12:g.12871228del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718295del , CM000674.2:g.12718295del GRCh38
NC_000012.11:g.12871229del , CM000674.1:g.12871229del GRCh37
NC_000012.10:g.12762496del NCBI36
NG_016341.1:g.5928del

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.456del ENSP00000507272.1:p.Lys153SerfsTer?
ENST00000682620.1:n.1631-530del
ENST00000684771.1:n.585-530del
ENST00000228872.9:c.456del MANE Select ENSP00000228872.4:p.Lys153SerfsTer?
ENST00000228872.8:c.456del ENSP00000228872.4:p.Lys153SerfsTer?
ENST00000396340.1:c.456del ENSP00000379629.1:p.Lys153SerfsTer19
ENST00000442489.1:c.193+242del ENSP00000407597.1:n.193+242del
ENST00000477087.1:n.155-530del
NM_004064.4:c.456del NP_004055.1:p.Lys153SerfsTer?
NM_004064.5:c.456del MANE Select NP_004055.1:p.Lys153SerfsTer?