Canonical Allele Identifier: CA2697559111
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 2768597
ClinVar RCV Id: RCV003510348

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718050_12718056del , CM000674.2:g.12718050_12718056del GRCh38
NC_000012.11:g.12870984_12870990del , CM000674.1:g.12870984_12870990del GRCh37
NC_000012.10:g.12762251_12762257del NCBI36
NG_016341.1:g.5683_5689del

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.211_217del ENSP00000507272.1:p.Glu71SerfsTer?
ENST00000682620.1:n.1631-775_1631-769del
ENST00000684771.1:n.585-775_585-769del
ENST00000228872.9:c.211_217del MANE Select ENSP00000228872.4:p.Glu71SerfsTer?
ENST00000228872.8:c.211_217del ENSP00000228872.4:p.Glu71SerfsTer?
ENST00000396340.1:c.211_217del ENSP00000379629.1:p.Glu71SerfsTer?
ENST00000442489.1:c.190_193+3del
ENST00000477087.1:n.155-775_155-769del
NM_004064.4:c.211_217del NP_004055.1:p.Glu71SerfsTer?
NM_004064.5:c.211_217del MANE Select NP_004055.1:p.Glu71SerfsTer?