Canonical Allele Identifier: CA684981118
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs1289193942

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718206_12718207del , CM000674.2:g.12718206_12718207del GRCh38
NC_000012.11:g.12871140_12871141del , CM000674.1:g.12871140_12871141del GRCh37
NC_000012.10:g.12762407_12762408del NCBI36
NG_016341.1:g.5839_5840del

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.367_368del ENSP00000507272.1:p.Ala123Ter
ENST00000682620.1:n.1631-619_1631-618del
ENST00000684771.1:n.585-619_585-618del
ENST00000228872.9:c.367_368del MANE Select ENSP00000228872.4:p.Ala123Ter
ENST00000228872.8:c.367_368del ENSP00000228872.4:p.Ala123Ter
ENST00000396340.1:c.367_368del ENSP00000379629.1:p.Ala123Ter
ENST00000442489.1:c.193+153_193+154del ENSP00000407597.1:n.193+153_193+154del
ENST00000477087.1:n.155-619_155-618del
NM_004064.4:c.367_368del NP_004055.1:p.Ala123Ter
NM_004064.5:c.367_368del MANE Select NP_004055.1:p.Ala123Ter