Canonical Allele Identifier: CA478845560
Gene: CDKN1B HGNC NCBI

Linked Data

COSMIC: COSM239280
MyVariant Identifiers: chr12:g.12871077del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718144del , CM000674.2:g.12718144del GRCh38
NC_000012.11:g.12871078del , CM000674.1:g.12871078del GRCh37
NC_000012.10:g.12762345del NCBI36
NG_016341.1:g.5777del

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.305del ENSP00000507272.1:p.Pro102ArgfsTer17
ENST00000682620.1:n.1631-681del
ENST00000684771.1:n.585-681del
ENST00000228872.9:c.305del MANE Select ENSP00000228872.4:p.Pro102ArgfsTer17
ENST00000228872.8:c.305del ENSP00000228872.4:p.Pro102ArgfsTer17
ENST00000396340.1:c.305del ENSP00000379629.1:p.Pro102ArgfsTer17
ENST00000442489.1:c.193+91del ENSP00000407597.1:n.193+91del
ENST00000477087.1:n.155-681del
NM_004064.4:c.305del NP_004055.1:p.Pro102ArgfsTer17
NM_004064.5:c.305del MANE Select NP_004055.1:p.Pro102ArgfsTer17