Canonical Allele Identifier: CA645576632
Gene: CDKN1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717918_12717919insGT , CM000674.2:g.12717918_12717919insGT GRCh38
NC_000012.11:g.12870852_12870853insGT , CM000674.1:g.12870852_12870853insGT GRCh37
NC_000012.10:g.12762119_12762120insGT NCBI36
NG_016341.1:g.5551_5552insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.79_80insGT ENSP00000507272.1:p.Ser27CysfsTer16
ENST00000682620.1:n.1631-907_1631-906insGT
ENST00000684771.1:n.585-907_585-906insGT
ENST00000228872.9:c.79_80insGT MANE Select ENSP00000228872.4:p.Ser27CysfsTer16
ENST00000228872.8:c.79_80insGT ENSP00000228872.4:p.Ser27CysfsTer16
ENST00000396340.1:c.79_80insGT ENSP00000379629.1:p.Ser27CysfsTer16
ENST00000442489.1:c.58_59insGT ENSP00000407597.1:p.Ser20CysfsTer16
ENST00000477087.1:n.155-907_155-906insGT
NM_004064.4:c.79_80insGT NP_004055.1:p.Ser27CysfsTer16
NM_004064.5:c.79_80insGT MANE Select NP_004055.1:p.Ser27CysfsTer16