Canonical Allele Identifier: CA2017047993
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs1946505117

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718533_12718539del , CM000674.2:g.12718533_12718539del GRCh38
NC_000012.11:g.12871467_12871473del , CM000674.1:g.12871467_12871473del GRCh37
NC_000012.10:g.12762734_12762740del NCBI36
NG_016341.1:g.6166_6172del

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.475+219_475+225del ENSP00000507272.1:n.475+219_475+225del
ENST00000682620.1:n.1631-292_1631-286del
ENST00000684771.1:n.585-292_585-286del
ENST00000228872.9:c.475+219_475+225del MANE Select ENSP00000228872.4:n.475+219_475+225del
ENST00000228872.8:c.475+219_475+225del ENSP00000228872.4:n.475+219_475+225del
ENST00000396340.1:c.475+219_475+225del ENSP00000379629.1:n.475+219_475+225del
ENST00000442489.1:c.194-292_194-286del ENSP00000407597.1:n.194-292_194-286del
ENST00000477087.1:n.155-292_155-286del
NM_004064.4:c.475+219_475+225del NP_004055.1:n.475+219_475+225del
NM_004064.5:c.475+219_475+225del MANE Select NP_004055.1:n.475+219_475+225del