Canonical Allele Identifier: CA2735573018

Gene: STK11

Linked Data

• dbSNP Id: rs2145406066

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207207_1207208insATTCAACTACTGAGGAG , CM000681.2:g.1207207_1207208insATTCAACTACTGAGGAG	GRCh38
NC_000019.9:g.1207206_1207207insATTCAACTACTGAGGAG , CM000681.1:g.1207206_1207207insATTCAACTACTGAGGAG	GRCh37
NC_000019.8:g.1158206_1158207insATTCAACTACTGAGGAG	NCBI36
NG_007460.2:g.22801_22802insATTCAACTACTGAGGAG , LRG_319:g.22801_22802insATTCAACTACTGAGGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.290+4_290+5insATTCAACTACTGAGGAG	ENSP00000490268.2:n.290+4_290+5insATTCAACTACTGAGGAG
ENST00000585748.3:c.-82-11210_-82-11209insATTCAACTACTGAGGAG	ENSP00000477641.2:n.-82-11210_-82-11209insATTCAACTACTGAGGAG
ENST00000585851.2:c.290+4_290+5insATTCAACTACTGAGGAG	ENSP00000467912.2:n.290+4_290+5insATTCAACTACTGAGGAG
ENST00000326873.12:c.290+4_290+5insATTCAACTACTGAGGAG MANE Select	ENSP00000324856.6:n.290+4_290+5insATTCAACTACTGAGGAG
ENST00000652231.1:c.290+4_290+5insATTCAACTACTGAGGAG	ENSP00000498804.1:n.290+4_290+5insATTCAACTACTGAGGAG
ENST00000326873.11:c.290+4_290+5insATTCAACTACTGAGGAG	ENSP00000324856.6:n.290+4_290+5insATTCAACTACTGAGGAG
ENST00000585748.2:c.-82-11210_-82-11209insATTCAACTACTGAGGAG	ENSP00000477641.1:n.-82-11210_-82-11209insATTCAACTACTGAGGAG
ENST00000585851.1:c.290+4_290+5insATTCAACTACTGAGGAG	ENSP00000467912.1:n.290+4_290+5insATTCAACTACTGAGGAG
ENST00000586243.5:c.290+4_290+5insATTCAACTACTGAGGAG	ENSP00000467240.2:n.290+4_290+5insATTCAACTACTGAGGAG
ENST00000586358.5:n.113+4_113+5insATTCAACTACTGAGGAG
ENST00000589152.5:n.380+4_380+5insATTCAACTACTGAGGAG
ENST00000593219.5:c.290+4_290+5insATTCAACTACTGAGGAG	ENSP00000466610.1:n.290+4_290+5insATTCAACTACTGAGGAG
NM_000455.4:c.290+4_290+5insATTCAACTACTGAGGAG , LRG_319t1:c.290+4_290+5insATTCAACTACTGAGGAG	NP_000446.1:n.290+4_290+5insATTCAACTACTGAGGAG
XM_005259617.1:c.290+4_290+5insATTCAACTACTGAGGAG	XP_005259674.1:n.290+4_290+5insATTCAACTACTGAGGAG
XM_005259618.3:c.290+4_290+5insATTCAACTACTGAGGAG	XP_005259675.1:n.290+4_290+5insATTCAACTACTGAGGAG
XM_011528209.1:c.-64+4_-64+5insATTCAACTACTGAGGAG	XP_011526511.1:n.-64+4_-64+5insATTCAACTACTGAGGAG
XR_936204.1:n.915+4_915+5insATTCAACTACTGAGGAG
XM_005259617.3:c.290+4_290+5insATTCAACTACTGAGGAG	XP_005259674.1:n.290+4_290+5insATTCAACTACTGAGGAG
XM_011528209.2:c.-64+4_-64+5insATTCAACTACTGAGGAG	XP_011526511.1:n.-64+4_-64+5insATTCAACTACTGAGGAG
XR_001753738.2:n.915+4_915+5insATTCAACTACTGAGGAG
XR_001753739.1:n.915+4_915+5insATTCAACTACTGAGGAG
XR_001753740.2:n.915+4_915+5insATTCAACTACTGAGGAG
NM_000455.5:c.290+4_290+5insATTCAACTACTGAGGAG MANE Select	NP_000446.1:n.290+4_290+5insATTCAACTACTGAGGAG