Canonical Allele Identifier: CA2580085208
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 2139814
ClinVar RCV Id: RCV003066692

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718238_12718248del , CM000674.2:g.12718238_12718248del GRCh38
NC_000012.11:g.12871172_12871182del , CM000674.1:g.12871172_12871182del GRCh37
NC_000012.10:g.12762439_12762449del NCBI36
NG_016341.1:g.5871_5881del

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.399_409del ENSP00000507272.1:p.Lys134ValfsTer?
ENST00000682620.1:n.1631-587_1631-577del
ENST00000684771.1:n.585-587_585-577del
ENST00000228872.9:c.399_409del MANE Select ENSP00000228872.4:p.Lys134ValfsTer?
ENST00000228872.8:c.399_409del ENSP00000228872.4:p.Lys134ValfsTer?
ENST00000396340.1:c.399_409del ENSP00000379629.1:p.Lys134ValfsTer27
ENST00000442489.1:c.193+185_193+195del ENSP00000407597.1:n.193+185_193+195del
ENST00000477087.1:n.155-587_155-577del
NM_004064.4:c.399_409del NP_004055.1:p.Lys134ValfsTer?
NM_004064.5:c.399_409del MANE Select NP_004055.1:p.Lys134ValfsTer?