Canonical Allele Identifier: CA915947918
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 820078
ClinVar RCV Id: RCV001013161
dbSNP Id: rs1592280877

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718017dup , CM000674.2:g.12718017dup GRCh38
NC_000012.11:g.12870951dup , CM000674.1:g.12870951dup GRCh37
NC_000012.10:g.12762218dup NCBI36
NG_016341.1:g.5650dup

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.178dup ENSP00000507272.1:p.Trp60LeufsTer?
ENST00000682620.1:n.1631-808dup
ENST00000684771.1:n.585-808dup
ENST00000228872.9:c.178dup MANE Select ENSP00000228872.4:p.Trp60LeufsTer?
ENST00000228872.8:c.178dup ENSP00000228872.4:p.Trp60LeufsTer?
ENST00000396340.1:c.178dup ENSP00000379629.1:p.Trp60LeufsTer?
ENST00000442489.1:c.157dup ENSP00000407597.1:p.Trp53LeufsTer?
ENST00000477087.1:n.155-808dup
NM_004064.4:c.178dup NP_004055.1:p.Trp60LeufsTer?
NM_004064.5:c.178dup MANE Select NP_004055.1:p.Trp60LeufsTer?