Canonical Allele Identifier: CA2317590309

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221227C= , CM000681.2:g.1221227C=	GRCh38
NC_000019.9:g.1221226C= , CM000681.1:g.1221226C=	GRCh37
NC_000019.8:g.1172226C=	NCBI36
NG_007460.2:g.36821C= , LRG_319:g.36821C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.749C=	ENSP00000490268.2:p.Thr250=
ENST00000585748.3:c.377C=	ENSP00000477641.2:p.Thr126=
ENST00000585851.2:c.575C=	ENSP00000467912.2:p.Thr192=
ENST00000326873.12:c.749C= MANE Select	ENSP00000324856.6:p.Thr250=
ENST00000652231.1:c.749C=	ENSP00000498804.1:p.Thr250=
ENST00000326873.11:c.749C=	ENSP00000324856.6:p.Thr250=
ENST00000586243.5:c.749C=	ENSP00000467240.2:p.Thr250=
ENST00000586358.5:n.647C=
ENST00000589152.5:n.839C=
ENST00000591133.2:n.720C=
NM_000455.4:c.749C= , LRG_319t1:c.749C=	NP_000446.1:p.Thr250=
XM_005259617.1:c.749C=	XP_005259674.1:p.Thr250=
XM_005259618.3:c.749C=	XP_005259675.1:p.Thr250=
XM_011528209.1:c.527C=	XP_011526511.1:p.Thr176=
XR_936204.1:n.1374C=
XM_005259617.3:c.749C=	XP_005259674.1:p.Thr250=
XM_011528209.2:c.527C=	XP_011526511.1:p.Thr176=
XR_001753738.2:n.1374C=
XR_001753739.1:n.1374C=
XR_001753740.2:n.1374C=
NM_000455.5:c.749C= MANE Select	NP_000446.1:p.Thr250=