Canonical Allele Identifier: CA2317591447

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1222997G= , CM000681.2:g.1222997G=	GRCh38
NC_000019.9:g.1222996G= , CM000681.1:g.1222996G=	GRCh37
NC_000019.8:g.1173996G=	NCBI36
NG_007460.2:g.38591G= , LRG_319:g.38591G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.933G=	ENSP00000490268.2:p.Lys311=
ENST00000585748.3:c.561G=	ENSP00000477641.2:p.Lys187=
ENST00000585851.2:c.759G=	ENSP00000467912.2:p.Lys253=
ENST00000326873.12:c.933G= MANE Select	ENSP00000324856.6:p.Lys311=
ENST00000652231.1:c.933G=	ENSP00000498804.1:p.Lys311=
ENST00000326873.11:c.933G=	ENSP00000324856.6:p.Lys311=
ENST00000586243.5:c.933G=	ENSP00000467240.2:p.Lys311=
ENST00000589152.5:n.1631G=
ENST00000591133.2:n.904G=
NM_000455.4:c.933G= , LRG_319t1:c.933G=	NP_000446.1:p.Lys311=
XM_005259617.1:c.933G=	XP_005259674.1:p.Lys311=
XM_005259618.3:c.933G=	XP_005259675.1:p.Lys311=
XM_011528209.1:c.711G=	XP_011526511.1:p.Lys237=
XR_936204.1:n.1709G=
XM_005259617.3:c.933G=	XP_005259674.1:p.Lys311=
XM_011528209.2:c.711G=	XP_011526511.1:p.Lys237=
XR_001753738.2:n.1739G=
XR_001753739.1:n.1739G=
XR_001753740.2:n.1709G=
NM_000455.5:c.933G= MANE Select	NP_000446.1:p.Lys311=