Canonical Allele Identifier: CA2317593652

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226465G= , CM000681.2:g.1226465G=	GRCh38
NC_000019.9:g.1226464G= , CM000681.1:g.1226464G=	GRCh37
NC_000019.8:g.1177464G=	NCBI36
NG_007460.2:g.42059G= , LRG_319:g.42059G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2721G=	ENSP00000490268.2:n.*2721G=
ENST00000585748.3:c.748G=	ENSP00000477641.2:p.Glu250=
ENST00000585851.2:c.946G=	ENSP00000467912.2:p.Glu316=
ENST00000326873.12:c.1120G= MANE Select	ENSP00000324856.6:p.Glu374=
ENST00000326873.11:c.1120G=	ENSP00000324856.6:p.Glu374=
ENST00000585465.2:n.2853G=
ENST00000586243.5:c.1120G=	ENSP00000467240.2:p.Glu374=
ENST00000589152.5:n.1818G=
NM_000455.4:c.1120G= , LRG_319t1:c.1120G=	NP_000446.1:p.Glu374=
XM_005259617.1:c.1115G=	XP_005259674.1:p.Arg372=
XM_011528209.1:c.893G=	XP_011526511.1:p.Arg298=
XM_005259617.3:c.1115G=	XP_005259674.1:p.Arg372=
XM_011528209.2:c.893G=	XP_011526511.1:p.Arg298=
XR_001753738.2:n.1926G=
XR_001753740.2:n.1896G=
NM_000455.5:c.1120G= MANE Select	NP_000446.1:p.Glu374=