Canonical Allele Identifier: CA2317589115

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219397G= , CM000681.2:g.1219397G=	GRCh38
NC_000019.9:g.1219396G= , CM000681.1:g.1219396G=	GRCh37
NC_000019.8:g.1170396G=	NCBI36
NG_007460.2:g.34991G= , LRG_319:g.34991G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.448G=	ENSP00000490268.2:p.Val150=
ENST00000585748.3:c.76G=	ENSP00000477641.2:p.Val26=
ENST00000585851.2:c.291-976G=	ENSP00000467912.2:n.291-976G=
ENST00000326873.12:c.448G= MANE Select	ENSP00000324856.6:p.Val150=
ENST00000652231.1:c.448G=	ENSP00000498804.1:p.Val150=
ENST00000326873.11:c.448G=	ENSP00000324856.6:p.Val150=
ENST00000585851.1:c.291-976G=	ENSP00000467912.1:n.291-976G=
ENST00000586243.5:c.448G=	ENSP00000467240.2:p.Val150=
ENST00000586358.5:n.271G=
ENST00000589152.5:n.538G=
NM_000455.4:c.448G= , LRG_319t1:c.448G=	NP_000446.1:p.Val150=
XM_005259617.1:c.448G=	XP_005259674.1:p.Val150=
XM_005259618.3:c.448G=	XP_005259675.1:p.Val150=
XM_011528209.1:c.226G=	XP_011526511.1:p.Val76=
XR_936204.1:n.1073G=
XM_005259617.3:c.448G=	XP_005259674.1:p.Val150=
XM_011528209.2:c.226G=	XP_011526511.1:p.Val76=
XR_001753738.2:n.1073G=
XR_001753739.1:n.1073G=
XR_001753740.2:n.1073G=
NM_000455.5:c.448G= MANE Select	NP_000446.1:p.Val150=