Canonical Allele Identifier: CA478845825
Gene: CDKN1B HGNC NCBI

Linked Data

COSMIC: COSM430695
MyVariant Identifiers: chr12:g.12871175del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718241del , CM000674.2:g.12718241del GRCh38
NC_000012.11:g.12871175del , CM000674.1:g.12871175del GRCh37
NC_000012.10:g.12762442del NCBI36
NG_016341.1:g.5874del

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.402del ENSP00000507272.1:p.Thr135LeufsTer10
ENST00000682620.1:n.1631-584del
ENST00000684771.1:n.585-584del
ENST00000228872.9:c.402del MANE Select ENSP00000228872.4:p.Thr135LeufsTer10
ENST00000228872.8:c.402del ENSP00000228872.4:p.Thr135LeufsTer10
ENST00000396340.1:c.402del ENSP00000379629.1:p.Thr135LeufsTer10
ENST00000442489.1:c.193+188del ENSP00000407597.1:n.193+188del
ENST00000477087.1:n.155-584del
NM_004064.4:c.402del NP_004055.1:p.Thr135LeufsTer10
NM_004064.5:c.402del MANE Select NP_004055.1:p.Thr135LeufsTer10
Search 100 bp 5'
Search 100 bp 3'