Canonical Allele Identifier: CA2317588500

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218398_1218400delinsCCT , CM000681.2:g.1218398_1218400delinsCCT	GRCh38
NC_000019.9:g.1218397_1218399delinsCCT , CM000681.1:g.1218397_1218399delinsCCT	GRCh37
NC_000019.8:g.1169397_1169399delinsCCT	NCBI36
NG_007460.2:g.33992_33994delinsCCT , LRG_319:g.33992_33994delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.291-19_291-17delinsCCT	ENSP00000490268.2:n.291-19_291-17delinsCCT
ENST00000585748.3:c.-82-19_-82-17delinsCCT	ENSP00000477641.2:n.-82-19_-82-17delinsCCT
ENST00000585851.2:c.291-1975_291-1973delinsCCT	ENSP00000467912.2:n.291-1975_291-1973delinsCCT
ENST00000326873.12:c.291-19_291-17delinsCCT MANE Select	ENSP00000324856.6:n.291-19_291-17delinsCCT
ENST00000652231.1:c.291-19_291-17delinsCCT	ENSP00000498804.1:n.291-19_291-17delinsCCT
ENST00000326873.11:c.291-19_291-17delinsCCT	ENSP00000324856.6:n.291-19_291-17delinsCCT
ENST00000585748.2:c.-82-19_-82-17delinsCCT	ENSP00000477641.1:n.-82-19_-82-17delinsCCT
ENST00000585851.1:c.291-1975_291-1973delinsCCT	ENSP00000467912.1:n.291-1975_291-1973delinsCCT
ENST00000586243.5:c.291-19_291-17delinsCCT	ENSP00000467240.2:n.291-19_291-17delinsCCT
ENST00000586358.5:n.114-19_114-17delinsCCT
ENST00000589152.5:n.381-19_381-17delinsCCT
ENST00000593219.5:c.*116-19_*116-17delinsCCT	ENSP00000466610.1:n.*116-19_*116-17delinsCCT
NM_000455.4:c.291-19_291-17delinsCCT , LRG_319t1:c.291-19_291-17delinsCCT	NP_000446.1:n.291-19_291-17delinsCCT
XM_005259617.1:c.291-19_291-17delinsCCT	XP_005259674.1:n.291-19_291-17delinsCCT
XM_005259618.3:c.291-19_291-17delinsCCT	XP_005259675.1:n.291-19_291-17delinsCCT
XM_011528209.1:c.69-19_69-17delinsCCT	XP_011526511.1:n.69-19_69-17delinsCCT
XR_936204.1:n.916-19_916-17delinsCCT
XM_005259617.3:c.291-19_291-17delinsCCT	XP_005259674.1:n.291-19_291-17delinsCCT
XM_011528209.2:c.69-19_69-17delinsCCT	XP_011526511.1:n.69-19_69-17delinsCCT
XR_001753738.2:n.916-19_916-17delinsCCT
XR_001753739.1:n.916-19_916-17delinsCCT
XR_001753740.2:n.916-19_916-17delinsCCT
NM_000455.5:c.291-19_291-17delinsCCT MANE Select	NP_000446.1:n.291-19_291-17delinsCCT