Canonical Allele Identifier: CA2317589061

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219330G= , CM000681.2:g.1219330G=	GRCh38
NC_000019.9:g.1219329G= , CM000681.1:g.1219329G=	GRCh37
NC_000019.8:g.1170329G=	NCBI36
NG_007460.2:g.34924G= , LRG_319:g.34924G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.381G=	ENSP00000490268.2:p.Met127=
ENST00000585748.3:c.9G=	ENSP00000477641.2:p.Met3=
ENST00000585851.2:c.291-1043G=	ENSP00000467912.2:n.291-1043G=
ENST00000326873.12:c.381G= MANE Select	ENSP00000324856.6:p.Met127=
ENST00000652231.1:c.381G=	ENSP00000498804.1:p.Met127=
ENST00000326873.11:c.381G=	ENSP00000324856.6:p.Met127=
ENST00000585748.2:c.9G=	ENSP00000477641.1:p.Met3=
ENST00000585851.1:c.291-1043G=	ENSP00000467912.1:n.291-1043G=
ENST00000586243.5:c.381G=	ENSP00000467240.2:p.Met127=
ENST00000586358.5:n.204G=
ENST00000589152.5:n.471G=
ENST00000593219.5:c.*206G=	ENSP00000466610.1:n.*206G=
NM_000455.4:c.381G= , LRG_319t1:c.381G=	NP_000446.1:p.Met127=
XM_005259617.1:c.381G=	XP_005259674.1:p.Met127=
XM_005259618.3:c.381G=	XP_005259675.1:p.Met127=
XM_011528209.1:c.159G=	XP_011526511.1:p.Met53=
XR_936204.1:n.1006G=
XM_005259617.3:c.381G=	XP_005259674.1:p.Met127=
XM_011528209.2:c.159G=	XP_011526511.1:p.Met53=
XR_001753738.2:n.1006G=
XR_001753739.1:n.1006G=
XR_001753740.2:n.1006G=
NM_000455.5:c.381G= MANE Select	NP_000446.1:p.Met127=