Canonical Allele Identifier: CA16043168
Gene: STK11 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 372523
COSMIC: COSM20857

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1221268_1221271del , CM000681.2:g.1221268_1221271del GRCh38
NC_000019.9:g.1221267_1221270del , CM000681.1:g.1221267_1221270del GRCh37
NC_000019.8:g.1172267_1172270del NCBI36
NG_007460.2:g.36862_36865del , LRG_319:g.36862_36865del

Transcript Alleles

HGVS Amino-acid change
NM_000455.4:c.790_793del , LRG_319t1:c.790_793del NP_000446.1:p.Phe264ArgfsTer22
XM_005259617.1:c.790_793del XP_005259674.1:p.Phe264ArgfsTer22
XM_005259618.3:c.790_793del XP_005259675.1:p.Phe264ArgfsTer22
XM_011528209.1:c.568_571del XP_011526511.1:p.Phe190ArgfsTer22
XR_936204.1:n.1415_1418del
XM_005259617.3:c.790_793del
XM_011528209.2:c.568_571del
XR_001753738.2:n.1415_1418del
XR_001753739.1:n.1415_1418del
XR_001753740.2:n.1415_1418del
ENST00000326873.11:c.790_793del ENSP00000324856.6:p.Phe264ArgfsTer22
ENST00000586243.5:c.790_793del ENSP00000467240.2:p.Phe264ArgfsTer22
ENST00000586358.5:n.688_691del
ENST00000589152.5:n.880_883del
ENST00000591133.2:n.761_764del