Canonical Allele Identifier: CA2017048066
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs1946507291

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718662_12718664del , CM000674.2:g.12718662_12718664del GRCh38
NC_000012.11:g.12871596_12871598del , CM000674.1:g.12871596_12871598del GRCh37
NC_000012.10:g.12762863_12762865del NCBI36
NG_016341.1:g.6295_6297del

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.476-163_476-161del ENSP00000507272.1:n.476-163_476-161del
ENST00000682620.1:n.1631-163_1631-161del
ENST00000684771.1:n.585-163_585-161del
ENST00000228872.9:c.476-163_476-161del MANE Select ENSP00000228872.4:n.476-163_476-161del
ENST00000228872.8:c.476-163_476-161del ENSP00000228872.4:n.476-163_476-161del
ENST00000396340.1:c.475+348_475+350del ENSP00000379629.1:n.475+348_475+350del
ENST00000442489.1:c.194-163_194-161del ENSP00000407597.1:n.194-163_194-161del
ENST00000477087.1:n.155-163_155-161del
NM_004064.4:c.476-163_476-161del NP_004055.1:n.476-163_476-161del
NM_004064.5:c.476-163_476-161del MANE Select NP_004055.1:n.476-163_476-161del