Canonical Allele Identifier: CA2617685676
Gene: CDKN1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718029_12718038del , CM000674.2:g.12718029_12718038del GRCh38
NC_000012.11:g.12870963_12870972del , CM000674.1:g.12870963_12870972del GRCh37
NC_000012.10:g.12762230_12762239del NCBI36
NG_016341.1:g.5662_5671del

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.190_199del ENSP00000507272.1:p.Phe64ThrfsTer4
ENST00000682620.1:n.1631-796_1631-787del
ENST00000684771.1:n.585-796_585-787del
ENST00000228872.9:c.190_199del MANE Select ENSP00000228872.4:p.Phe64ThrfsTer4
ENST00000228872.8:c.190_199del ENSP00000228872.4:p.Phe64ThrfsTer4
ENST00000396340.1:c.190_199del ENSP00000379629.1:p.Phe64ThrfsTer4
ENST00000442489.1:c.169_178del ENSP00000407597.1:p.Phe57ThrfsTer4
ENST00000477087.1:n.155-796_155-787del
NM_004064.4:c.190_199del NP_004055.1:p.Phe64ThrfsTer4
NM_004064.5:c.190_199del MANE Select NP_004055.1:p.Phe64ThrfsTer4