Canonical Allele Identifier: CA022877
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 182913
dbSNP Id: rs587782424

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1219351_1219352del , CM000681.2:g.1219351_1219352del GRCh38
NC_000019.9:g.1219350_1219351del , CM000681.1:g.1219350_1219351del GRCh37
NC_000019.8:g.1170350_1170351del NCBI36
NG_007460.2:g.34945_34946del , LRG_319:g.34945_34946del

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.402_403del ENSP00000490268.2:p.Cys134TrpfsTer28
ENST00000585748.3:c.30_31del ENSP00000477641.2:p.Cys10TrpfsTer28
ENST00000585851.2:c.291-1022_291-1021del ENSP00000467912.2:n.291-1022_291-1021del
ENST00000326873.12:c.402_403del MANE Select ENSP00000324856.6:p.Cys134TrpfsTer28
ENST00000652231.1:c.402_403del ENSP00000498804.1:p.Cys134TrpfsTer28
ENST00000326873.11:c.402_403del ENSP00000324856.6:p.Cys134TrpfsTer28
ENST00000585748.2:c.30_31del ENSP00000477641.1:p.Cys10TrpfsTer?
ENST00000585851.1:c.291-1022_291-1021del ENSP00000467912.1:n.291-1022_291-1021del
ENST00000586243.5:c.402_403del ENSP00000467240.2:p.Cys134TrpfsTer28
ENST00000586358.5:n.225_226del
ENST00000589152.5:n.492_493del
ENST00000593219.5:c.*227_*228del ENSP00000466610.1:n.*227_*228del
NM_000455.4:c.402_403del , LRG_319t1:c.402_403del NP_000446.1:p.Cys134TrpfsTer28
XM_005259617.1:c.402_403del XP_005259674.1:p.Cys134TrpfsTer28
XM_005259618.3:c.402_403del XP_005259675.1:p.Cys134TrpfsTer28
XM_011528209.1:c.180_181del XP_011526511.1:p.Cys60TrpfsTer28
XR_936204.1:n.1027_1028del
XM_005259617.3:c.402_403del XP_005259674.1:p.Cys134TrpfsTer28
XM_011528209.2:c.180_181del XP_011526511.1:p.Cys60TrpfsTer28
XR_001753738.2:n.1027_1028del
XR_001753739.1:n.1027_1028del
XR_001753740.2:n.1027_1028del
NM_000455.5:c.402_403del MANE Select NP_000446.1:p.Cys134TrpfsTer28