Canonical Allele Identifier: CA2695227934

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220649del , CM000681.2:g.1220649del	GRCh38
NC_000019.9:g.1220648del , CM000681.1:g.1220648del	GRCh37
NC_000019.8:g.1171648del	NCBI36
NG_007460.2:g.36243del , LRG_319:g.36243del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.666del	ENSP00000490268.2:p.Glu223ArgfsTer?
ENST00000585748.3:c.294del	ENSP00000477641.2:p.Glu99ArgfsTer?
ENST00000585851.2:c.492del	ENSP00000467912.2:p.Glu165ArgfsTer?
ENST00000326873.12:c.666del MANE Select	ENSP00000324856.6:p.Glu223ArgfsTer?
ENST00000652231.1:c.666del	ENSP00000498804.1:p.Glu223ArgfsTer?
ENST00000326873.11:c.666del	ENSP00000324856.6:p.Glu223ArgfsTer?
ENST00000586243.5:c.666del	ENSP00000467240.2:p.Glu223ArgfsTer?
ENST00000586358.5:n.564del
ENST00000589152.5:n.756del
ENST00000591133.2:n.637del
NM_000455.4:c.666del , LRG_319t1:c.666del	NP_000446.1:p.Glu223ArgfsTer?
XM_005259617.1:c.666del	XP_005259674.1:p.Glu223ArgfsTer?
XM_005259618.3:c.666del	XP_005259675.1:p.Glu223ArgfsTer?
XM_011528209.1:c.444del	XP_011526511.1:p.Glu149ArgfsTer?
XR_936204.1:n.1291del
XM_005259617.3:c.666del	XP_005259674.1:p.Glu223ArgfsTer?
XM_011528209.2:c.444del	XP_011526511.1:p.Glu149ArgfsTer?
XR_001753738.2:n.1291del
XR_001753739.1:n.1291del
XR_001753740.2:n.1291del
NM_000455.5:c.666del MANE Select	NP_000446.1:p.Glu223ArgfsTer?