Canonical Allele Identifier: CA2317588502
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1218399_1218400delinsCT , CM000681.2:g.1218399_1218400delinsCT GRCh38
NC_000019.9:g.1218398_1218399delinsCT , CM000681.1:g.1218398_1218399delinsCT GRCh37
NC_000019.8:g.1169398_1169399delinsCT NCBI36
NG_007460.2:g.33993_33994delinsCT , LRG_319:g.33993_33994delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.291-18_291-17delinsCT ENSP00000490268.2:n.291-18_291-17delinsCT
ENST00000585748.3:c.-82-18_-82-17delinsCT ENSP00000477641.2:n.-82-18_-82-17delinsCT
ENST00000585851.2:c.291-1974_291-1973delinsCT ENSP00000467912.2:n.291-1974_291-1973delinsCT
ENST00000326873.12:c.291-18_291-17delinsCT MANE Select ENSP00000324856.6:n.291-18_291-17delinsCT
ENST00000652231.1:c.291-18_291-17delinsCT ENSP00000498804.1:n.291-18_291-17delinsCT
ENST00000326873.11:c.291-18_291-17delinsCT ENSP00000324856.6:n.291-18_291-17delinsCT
ENST00000585748.2:c.-82-18_-82-17delinsCT ENSP00000477641.1:n.-82-18_-82-17delinsCT
ENST00000585851.1:c.291-1974_291-1973delinsCT ENSP00000467912.1:n.291-1974_291-1973delinsCT
ENST00000586243.5:c.291-18_291-17delinsCT ENSP00000467240.2:n.291-18_291-17delinsCT
ENST00000586358.5:n.114-18_114-17delinsCT
ENST00000589152.5:n.381-18_381-17delinsCT
ENST00000593219.5:c.*116-18_*116-17delinsCT ENSP00000466610.1:n.*116-18_*116-17delinsCT
NM_000455.4:c.291-18_291-17delinsCT , LRG_319t1:c.291-18_291-17delinsCT NP_000446.1:n.291-18_291-17delinsCT
XM_005259617.1:c.291-18_291-17delinsCT XP_005259674.1:n.291-18_291-17delinsCT
XM_005259618.3:c.291-18_291-17delinsCT XP_005259675.1:n.291-18_291-17delinsCT
XM_011528209.1:c.69-18_69-17delinsCT XP_011526511.1:n.69-18_69-17delinsCT
XR_936204.1:n.916-18_916-17delinsCT
XM_005259617.3:c.291-18_291-17delinsCT XP_005259674.1:n.291-18_291-17delinsCT
XM_011528209.2:c.69-18_69-17delinsCT XP_011526511.1:n.69-18_69-17delinsCT
XR_001753738.2:n.916-18_916-17delinsCT
XR_001753739.1:n.916-18_916-17delinsCT
XR_001753740.2:n.916-18_916-17delinsCT
NM_000455.5:c.291-18_291-17delinsCT MANE Select NP_000446.1:n.291-18_291-17delinsCT