Canonical Allele Identifier: CA022918
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 7449
dbSNP Id: rs397518440

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1219367del , CM000681.2:g.1219367del GRCh38
NC_000019.9:g.1219366del , CM000681.1:g.1219366del GRCh37
NC_000019.8:g.1170366del NCBI36
NG_007460.2:g.34961del , LRG_319:g.34961del

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.418del ENSP00000490268.2:p.Leu140TrpfsTer21
ENST00000585748.3:c.46del ENSP00000477641.2:p.Leu16TrpfsTer21
ENST00000585851.2:c.291-1006del ENSP00000467912.2:n.291-1006del
ENST00000326873.12:c.418del MANE Select ENSP00000324856.6:p.Leu140TrpfsTer21
ENST00000652231.1:c.418del ENSP00000498804.1:p.Leu140TrpfsTer21
ENST00000326873.11:c.418del ENSP00000324856.6:p.Leu140TrpfsTer21
ENST00000585748.2:c.46del ENSP00000477641.1:p.Leu16TrpfsTer?
ENST00000585851.1:c.291-1006del ENSP00000467912.1:n.291-1006del
ENST00000586243.5:c.418del ENSP00000467240.2:p.Leu140TrpfsTer21
ENST00000586358.5:n.241del
ENST00000589152.5:n.508del
NM_000455.4:c.418del , LRG_319t1:c.418del NP_000446.1:p.Leu140TrpfsTer21
XM_005259617.1:c.418del XP_005259674.1:p.Leu140TrpfsTer21
XM_005259618.3:c.418del XP_005259675.1:p.Leu140TrpfsTer21
XM_011528209.1:c.196del XP_011526511.1:p.Leu66TrpfsTer21
XR_936204.1:n.1043del
XM_005259617.3:c.418del XP_005259674.1:p.Leu140TrpfsTer21
XM_011528209.2:c.196del XP_011526511.1:p.Leu66TrpfsTer21
XR_001753738.2:n.1043del
XR_001753739.1:n.1043del
XR_001753740.2:n.1043del
NM_000455.5:c.418del MANE Select NP_000446.1:p.Leu140TrpfsTer21