Canonical Allele Identifier: CA2017047765
Gene: CDKN1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718227_12718230delinsTTGG , CM000674.2:g.12718227_12718230delinsTTGG GRCh38
NC_000012.11:g.12871161_12871164delinsTTGG , CM000674.1:g.12871161_12871164delinsTTGG GRCh37
NC_000012.10:g.12762428_12762431delinsTTGG NCBI36
NG_016341.1:g.5860_5863delinsTTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.388_391delinsTTGG ENSP00000507272.1:p.Leu130=
ENST00000682620.1:n.1631-598_1631-595delinsTTGG
ENST00000684771.1:n.585-598_585-595delinsTTGG
ENST00000228872.9:c.388_391delinsTTGG MANE Select ENSP00000228872.4:p.Leu130=
ENST00000228872.8:c.388_391delinsTTGG ENSP00000228872.4:p.Leu130=
ENST00000396340.1:c.388_391delinsTTGG ENSP00000379629.1:p.Leu130=
ENST00000442489.1:c.193+174_193+177delinsTTGG ENSP00000407597.1:n.193+174_193+177delins...
ENST00000477087.1:n.155-598_155-595delinsTTGG
NM_004064.4:c.388_391delinsTTGG NP_004055.1:p.Leu130=
NM_004064.5:c.388_391delinsTTGG MANE Select NP_004055.1:p.Leu130=