Canonical Allele Identifier: CA2575083658
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 2705032
ClinVar RCV Id: RCV003510619

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718114del , CM000674.2:g.12718114del GRCh38
NC_000012.11:g.12871048del , CM000674.1:g.12871048del GRCh37
NC_000012.10:g.12762315del NCBI36
NG_016341.1:g.5747del

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.275del ENSP00000507272.1:p.Pro92ArgfsTer27
ENST00000682620.1:n.1631-711del
ENST00000684771.1:n.585-711del
ENST00000228872.9:c.275del MANE Select ENSP00000228872.4:p.Pro92ArgfsTer27
ENST00000228872.8:c.275del ENSP00000228872.4:p.Pro92ArgfsTer27
ENST00000396340.1:c.275del ENSP00000379629.1:p.Pro92ArgfsTer27
ENST00000442489.1:c.193+61del ENSP00000407597.1:n.193+61del
ENST00000477087.1:n.155-711del
NM_004064.4:c.275del NP_004055.1:p.Pro92ArgfsTer27
NM_004064.5:c.275del MANE Select NP_004055.1:p.Pro92ArgfsTer27