Canonical Allele Identifier: CA2317593694

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226513G= , CM000681.2:g.1226513G=	GRCh38
NC_000019.9:g.1226512G= , CM000681.1:g.1226512G=	GRCh37
NC_000019.8:g.1177512G=	NCBI36
NG_007460.2:g.42107G= , LRG_319:g.42107G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2769G=	ENSP00000490268.2:n.*2769G=
ENST00000585748.3:c.796G=	ENSP00000477641.2:p.Val266=
ENST00000585851.2:c.994G=	ENSP00000467912.2:p.Val332=
ENST00000326873.12:c.1168G= MANE Select	ENSP00000324856.6:p.Val390=
ENST00000326873.11:c.1168G=	ENSP00000324856.6:p.Val390=
ENST00000585465.2:n.2901G=
ENST00000586243.5:c.1168G=	ENSP00000467240.2:p.Val390=
ENST00000589152.5:n.1866G=
NM_000455.4:c.1168G= , LRG_319t1:c.1168G=	NP_000446.1:p.Val390=
XM_005259617.1:c.1163G=	XP_005259674.1:p.Arg388=
XM_011528209.1:c.941G=	XP_011526511.1:p.Arg314=
XM_005259617.3:c.1163G=	XP_005259674.1:p.Arg388=
XM_011528209.2:c.941G=	XP_011526511.1:p.Arg314=
XR_001753738.2:n.1974G=
XR_001753740.2:n.1944G=
NM_000455.5:c.1168G= MANE Select	NP_000446.1:p.Val390=