Canonical Allele Identifier: CA9039444
Gene: STK11 HGNC NCBI

Linked Data

dbSNP Id: rs769089752

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1206890_1206891insC , CM000681.2:g.1206890_1206891insC GRCh38
NC_000019.9:g.1206889_1206890insC , CM000681.1:g.1206889_1206890insC GRCh37
NC_000019.8:g.1157889_1157890insC NCBI36
NG_007460.2:g.22484_22485insC , LRG_319:g.22484_22485insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.-24_-23insC ENSP00000490268.2:n.-24_-23insC
ENST00000585748.3:c.-82-11527_-82-11526insC ENSP00000477641.2:n.-82-11527_-82-11526insC
ENST00000585851.2:c.-24_-23insC ENSP00000467912.2:n.-24_-23insC
ENST00000326873.12:c.-24_-23insC MANE Select ENSP00000324856.6:n.-24_-23insC
ENST00000652231.1:c.-24_-23insC ENSP00000498804.1:n.-24_-23insC
ENST00000326873.11:c.-24_-23insC ENSP00000324856.6:n.-24_-23insC
ENST00000585748.2:c.-82-11527_-82-11526insC ENSP00000477641.1:n.-82-11527_-82-11526insC
ENST00000585851.1:c.-24_-23insC ENSP00000467912.1:n.-24_-23insC
ENST00000586243.5:c.-24_-23insC ENSP00000467240.2:n.-24_-23insC
ENST00000589152.5:n.67_68insC
ENST00000593219.5:c.-24_-23insC ENSP00000466610.1:n.-24_-23insC
NM_000455.4:c.-24_-23insC , LRG_319t1:c.-24_-23insC NP_000446.1:n.-24_-23insC
XM_005259617.1:c.-24_-23insC XP_005259674.1:n.-24_-23insC
XM_005259618.3:c.-24_-23insC XP_005259675.1:n.-24_-23insC
XM_011528209.1:c.-377_-376insC XP_011526511.1:n.-377_-376insC
XR_936204.1:n.602_603insC
XM_005259617.3:c.-24_-23insC XP_005259674.1:n.-24_-23insC
XM_011528209.2:c.-377_-376insC XP_011526511.1:n.-377_-376insC
XR_001753738.2:n.602_603insC
XR_001753739.1:n.602_603insC
XR_001753740.2:n.602_603insC
NM_000455.5:c.-24_-23insC MANE Select NP_000446.1:n.-24_-23insC