Canonical Allele Identifier: CA658797847

Gene: CDKN1B

Linked Data

• ClinVar Variation Id: 536842
• ClinVar RCV Id: RCV000645519
• dbSNP Id: rs1555085568

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718091_12718092delinsCT , CM000674.2:g.12718091_12718092delinsCT	GRCh38
NC_000012.11:g.12871025_12871026delinsCT , CM000674.1:g.12871025_12871026delinsCT	GRCh37
NC_000012.10:g.12762292_12762293delinsCT	NCBI36
NG_016341.1:g.5724_5725delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.252_253delinsCT	ENSP00000507272.1:p.Leu84_Pro85delinsPheSer
ENST00000682620.1:n.1631-734_1631-733delinsCT
ENST00000684771.1:n.585-734_585-733delinsCT
ENST00000228872.9:c.252_253delinsCT MANE Select	ENSP00000228872.4:p.Leu84_Pro85delinsPheSer
ENST00000228872.8:c.252_253delinsCT	ENSP00000228872.4:p.Leu84_Pro85delinsPheSer
ENST00000396340.1:c.252_253delinsCT	ENSP00000379629.1:p.Leu84_Pro85delinsPheSer
ENST00000442489.1:c.193+38_193+39delinsCT	ENSP00000407597.1:n.193+38_193+39delinsCT
ENST00000477087.1:n.155-734_155-733delinsCT
NM_004064.4:c.252_253delinsCT	NP_004055.1:p.Leu84_Pro85delinsPheSer
NM_004064.5:c.252_253delinsCT MANE Select	NP_004055.1:p.Leu84_Pro85delinsPheSer