Canonical Allele Identifier: CA2317588637

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218598A= , CM000681.2:g.1218598A=	GRCh38
NC_000019.9:g.1218597A= , CM000681.1:g.1218597A=	GRCh37
NC_000019.8:g.1169597A=	NCBI36
NG_007460.2:g.34192A= , LRG_319:g.34192A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.374+98A=	ENSP00000490268.2:n.374+98A=
ENST00000585748.3:c.2+98A=	ENSP00000477641.2:n.2+98A=
ENST00000585851.2:c.291-1775A=	ENSP00000467912.2:n.291-1775A=
ENST00000326873.12:c.374+98A= MANE Select	ENSP00000324856.6:n.374+98A=
ENST00000652231.1:c.374+98A=	ENSP00000498804.1:n.374+98A=
ENST00000326873.11:c.374+98A=	ENSP00000324856.6:n.374+98A=
ENST00000585748.2:c.2+98A=	ENSP00000477641.1:n.2+98A=
ENST00000585851.1:c.291-1775A=	ENSP00000467912.1:n.291-1775A=
ENST00000586243.5:c.374+98A=	ENSP00000467240.2:n.374+98A=
ENST00000586358.5:n.197+98A=
ENST00000589152.5:n.464+98A=
ENST00000593219.5:c.*199+98A=	ENSP00000466610.1:n.*199+98A=
NM_000455.4:c.374+98A= , LRG_319t1:c.374+98A=	NP_000446.1:n.374+98A=
XM_005259617.1:c.374+98A=	XP_005259674.1:n.374+98A=
XM_005259618.3:c.374+98A=	XP_005259675.1:n.374+98A=
XM_011528209.1:c.152+98A=	XP_011526511.1:n.152+98A=
XR_936204.1:n.999+98A=
XM_005259617.3:c.374+98A=	XP_005259674.1:n.374+98A=
XM_011528209.2:c.152+98A=	XP_011526511.1:n.152+98A=
XR_001753738.2:n.999+98A=
XR_001753739.1:n.999+98A=
XR_001753740.2:n.999+98A=
NM_000455.5:c.374+98A= MANE Select	NP_000446.1:n.374+98A=