Canonical Allele Identifier: CA2317593761

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226590C= , CM000681.2:g.1226590C=	GRCh38
NC_000019.9:g.1226589C= , CM000681.1:g.1226589C=	GRCh37
NC_000019.8:g.1177589C=	NCBI36
NG_007460.2:g.42184C= , LRG_319:g.42184C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2846C=	ENSP00000490268.2:n.*2846C=
ENST00000585748.3:c.873C=	ENSP00000477641.2:p.Arg291=
ENST00000585851.2:c.1071C=	ENSP00000467912.2:p.Arg357=
ENST00000326873.12:c.1245C= MANE Select	ENSP00000324856.6:p.Arg415=
ENST00000326873.11:c.1245C=	ENSP00000324856.6:p.Arg415=
ENST00000585465.2:n.2978C=
ENST00000586243.5:c.1244C=	ENSP00000467240.2:p.Ala415=
ENST00000589152.5:n.1943C=
NM_000455.4:c.1245C= , LRG_319t1:c.1245C=	NP_000446.1:p.Arg415=
XM_005259617.1:c.1240C=	XP_005259674.1:p.Gln414=
XM_011528209.1:c.1018C=	XP_011526511.1:p.Gln340=
XM_005259617.3:c.1240C=	XP_005259674.1:p.Gln414=
XM_011528209.2:c.1018C=	XP_011526511.1:p.Gln340=
XR_001753738.2:n.2051C=
XR_001753740.2:n.2021C=
NM_000455.5:c.1245C= MANE Select	NP_000446.1:p.Arg415=