Canonical Allele Identifier: CA2317593722

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226543C= , CM000681.2:g.1226543C=	GRCh38
NC_000019.9:g.1226542C= , CM000681.1:g.1226542C=	GRCh37
NC_000019.8:g.1177542C=	NCBI36
NG_007460.2:g.42137C= , LRG_319:g.42137C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2799C=	ENSP00000490268.2:n.*2799C=
ENST00000585748.3:c.826C=	ENSP00000477641.2:p.Leu276=
ENST00000585851.2:c.1024C=	ENSP00000467912.2:p.Leu342=
ENST00000326873.12:c.1198C= MANE Select	ENSP00000324856.6:p.Leu400=
ENST00000326873.11:c.1198C=	ENSP00000324856.6:p.Leu400=
ENST00000585465.2:n.2931C=
ENST00000586243.5:c.1198C=	ENSP00000467240.2:p.Leu400=
ENST00000589152.5:n.1896C=
NM_000455.4:c.1198C= , LRG_319t1:c.1198C=	NP_000446.1:p.Leu400=
XM_005259617.1:c.1193C=	XP_005259674.1:p.Ala398=
XM_011528209.1:c.971C=	XP_011526511.1:p.Ala324=
XM_005259617.3:c.1193C=	XP_005259674.1:p.Ala398=
XM_011528209.2:c.971C=	XP_011526511.1:p.Ala324=
XR_001753738.2:n.2004C=
XR_001753740.2:n.1974C=
NM_000455.5:c.1198C= MANE Select	NP_000446.1:p.Leu400=