Canonical Allele Identifier: CA1139662516
Gene: CDKN1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718120_12718121insT , CM000674.2:g.12718120_12718121insT GRCh38
NC_000012.11:g.12871054_12871055insT , CM000674.1:g.12871054_12871055insT GRCh37
NC_000012.10:g.12762321_12762322insT NCBI36
NG_016341.1:g.5753_5754insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.281_282insT ENSP00000507272.1:p.Lys96GlnfsTer29
ENST00000682620.1:n.1631-705_1631-704insT
ENST00000684771.1:n.585-705_585-704insT
ENST00000228872.9:c.281_282insT MANE Select ENSP00000228872.4:p.Lys96GlnfsTer29
ENST00000228872.8:c.281_282insT ENSP00000228872.4:p.Lys96GlnfsTer29
ENST00000396340.1:c.281_282insT ENSP00000379629.1:p.Lys96GlnfsTer29
ENST00000442489.1:c.193+67_193+68insT ENSP00000407597.1:n.193+67_193+68insT
ENST00000477087.1:n.155-705_155-704insT
NM_004064.4:c.281_282insT NP_004055.1:p.Lys96GlnfsTer29
NM_004064.5:c.281_282insT MANE Select NP_004055.1:p.Lys96GlnfsTer29