Canonical Allele Identifier: CA2580085202
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1987501
ClinVar RCV Id: RCV002776032

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718167_12718178del , CM000674.2:g.12718167_12718178del GRCh38
NC_000012.11:g.12871101_12871112del , CM000674.1:g.12871101_12871112del GRCh37
NC_000012.10:g.12762368_12762379del NCBI36
NG_016341.1:g.5800_5811del

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.328_339del ENSP00000507272.1:p.Ser110_Arg113del
ENST00000682620.1:n.1631-658_1631-647del
ENST00000684771.1:n.585-658_585-647del
ENST00000228872.9:c.328_339del MANE Select ENSP00000228872.4:p.Ser110_Arg113del
ENST00000228872.8:c.328_339del ENSP00000228872.4:p.Ser110_Arg113del
ENST00000396340.1:c.328_339del ENSP00000379629.1:p.Ser110_Arg113del
ENST00000442489.1:c.193+114_193+125del ENSP00000407597.1:n.193+114_193+125del
ENST00000477087.1:n.155-658_155-647del
NM_004064.4:c.328_339del NP_004055.1:p.Ser110_Arg113del
NM_004064.5:c.328_339del MANE Select NP_004055.1:p.Ser110_Arg113del