Canonical Allele Identifier: CA2317591559

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223133G= , CM000681.2:g.1223133G=	GRCh38
NC_000019.9:g.1223132G= , CM000681.1:g.1223132G=	GRCh37
NC_000019.8:g.1174132G=	NCBI36
NG_007460.2:g.38727G= , LRG_319:g.38727G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1069G=	ENSP00000490268.2:p.Glu357=
ENST00000585748.3:c.697G=	ENSP00000477641.2:p.Glu233=
ENST00000585851.2:c.895G=	ENSP00000467912.2:p.Glu299=
ENST00000326873.12:c.1069G= MANE Select	ENSP00000324856.6:p.Glu357=
ENST00000652231.1:c.1069G=	ENSP00000498804.1:p.Glu357=
ENST00000326873.11:c.1069G=	ENSP00000324856.6:p.Glu357=
ENST00000586243.5:c.1069G=	ENSP00000467240.2:p.Glu357=
ENST00000589152.5:n.1767G=
NM_000455.4:c.1069G= , LRG_319t1:c.1069G=	NP_000446.1:p.Glu357=
XM_005259617.1:c.1069G=	XP_005259674.1:p.Glu357=
XM_005259618.3:c.1069G=	XP_005259675.1:p.Glu357=
XM_011528209.1:c.847G=	XP_011526511.1:p.Glu283=
XR_936204.1:n.1845G=
XM_005259617.3:c.1069G=	XP_005259674.1:p.Glu357=
XM_011528209.2:c.847G=	XP_011526511.1:p.Glu283=
XR_001753738.2:n.1875G=
XR_001753739.1:n.1875G=
XR_001753740.2:n.1845G=
NM_000455.5:c.1069G= MANE Select	NP_000446.1:p.Glu357=