Canonical Allele Identifier: CA2317581770

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207226_1207231delinsGGGGCC , CM000681.2:g.1207226_1207231delinsGGGGCC	GRCh38
NC_000019.9:g.1207225_1207230delinsGGGGCC , CM000681.1:g.1207225_1207230delinsGGGGCC	GRCh37
NC_000019.8:g.1158225_1158230delinsGGGGCC	NCBI36
NG_007460.2:g.22820_22825delinsGGGGCC , LRG_319:g.22820_22825delinsGGGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.290+23_290+28delinsGGGGCC	ENSP00000490268.2:n.290+23_290+28delinsGGGGCC
ENST00000585748.3:c.-82-11191_-82-11186delinsGGGGCC	ENSP00000477641.2:n.-82-11191_-82-11186delinsGGGGCC
ENST00000585851.2:c.290+23_290+28delinsGGGGCC	ENSP00000467912.2:n.290+23_290+28delinsGGGGCC
ENST00000326873.12:c.290+23_290+28delinsGGGGCC MANE Select	ENSP00000324856.6:n.290+23_290+28delinsGGGGCC
ENST00000652231.1:c.290+23_290+28delinsGGGGCC	ENSP00000498804.1:n.290+23_290+28delinsGGGGCC
ENST00000326873.11:c.290+23_290+28delinsGGGGCC	ENSP00000324856.6:n.290+23_290+28delinsGGGGCC
ENST00000585748.2:c.-82-11191_-82-11186delinsGGGGCC	ENSP00000477641.1:n.-82-11191_-82-11186delinsGGGGCC
ENST00000585851.1:c.290+23_290+28delinsGGGGCC	ENSP00000467912.1:n.290+23_290+28delinsGGGGCC
ENST00000586243.5:c.290+23_290+28delinsGGGGCC	ENSP00000467240.2:n.290+23_290+28delinsGGGGCC
ENST00000586358.5:n.113+23_113+28delinsGGGGCC
ENST00000589152.5:n.380+23_380+28delinsGGGGCC
ENST00000593219.5:c.290+23_290+28delinsGGGGCC	ENSP00000466610.1:n.290+23_290+28delinsGGGGCC
NM_000455.4:c.290+23_290+28delinsGGGGCC , LRG_319t1:c.290+23_290+28delinsGGGGCC	NP_000446.1:n.290+23_290+28delinsGGGGCC
XM_005259617.1:c.290+23_290+28delinsGGGGCC	XP_005259674.1:n.290+23_290+28delinsGGGGCC
XM_005259618.3:c.290+23_290+28delinsGGGGCC	XP_005259675.1:n.290+23_290+28delinsGGGGCC
XM_011528209.1:c.-64+23_-64+28delinsGGGGCC	XP_011526511.1:n.-64+23_-64+28delinsGGGGCC
XR_936204.1:n.915+23_915+28delinsGGGGCC
XM_005259617.3:c.290+23_290+28delinsGGGGCC	XP_005259674.1:n.290+23_290+28delinsGGGGCC
XM_011528209.2:c.-64+23_-64+28delinsGGGGCC	XP_011526511.1:n.-64+23_-64+28delinsGGGGCC
XR_001753738.2:n.915+23_915+28delinsGGGGCC
XR_001753739.1:n.915+23_915+28delinsGGGGCC
XR_001753740.2:n.915+23_915+28delinsGGGGCC
NM_000455.5:c.290+23_290+28delinsGGGGCC MANE Select	NP_000446.1:n.290+23_290+28delinsGGGGCC