Canonical Allele Identifier: CA478845411
Gene: CDKN1B HGNC NCBI

Linked Data

COSMIC: COSM392594
MyVariant Identifiers: chr12:g.12871010del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718077del , CM000674.2:g.12718077del GRCh38
NC_000012.11:g.12871011del , CM000674.1:g.12871011del GRCh37
NC_000012.10:g.12762278del NCBI36
NG_016341.1:g.5710del

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.238del ENSP00000507272.1:p.Glu80ArgfsTer?
ENST00000682620.1:n.1631-748del
ENST00000684771.1:n.585-748del
ENST00000228872.9:c.238del MANE Select ENSP00000228872.4:p.Glu80ArgfsTer?
ENST00000228872.8:c.238del ENSP00000228872.4:p.Glu80ArgfsTer?
ENST00000396340.1:c.238del ENSP00000379629.1:p.Glu80ArgfsTer?
ENST00000442489.1:c.193+24del ENSP00000407597.1:n.193+24del
ENST00000477087.1:n.155-748del
NM_004064.4:c.238del NP_004055.1:p.Glu80ArgfsTer?
NM_004064.5:c.238del MANE Select NP_004055.1:p.Glu80ArgfsTer?