Canonical Allele Identifier: CA2317589774

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220435A= , CM000681.2:g.1220435A=	GRCh38
NC_000019.9:g.1220434A= , CM000681.1:g.1220434A=	GRCh37
NC_000019.8:g.1171434A=	NCBI36
NG_007460.2:g.36029A= , LRG_319:g.36029A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.527A= MANE Select	NP_000446.1:p.Asp176=
ENST00000326873.12:c.527A= MANE Select	ENSP00000324856.6:p.Asp176=
NM_000455.4:c.527A= , LRG_319t1:c.527A=	NP_000446.1:p.Asp176=
ENST00000326873.11:c.527A=	ENSP00000324856.6:p.Asp176=
ENST00000585465.3:c.527A=	ENSP00000490268.2:p.Asp176=
ENST00000585748.3:c.155A=	ENSP00000477641.2:p.Asp52=
ENST00000585851.1:c.353A=	ENSP00000467912.1:p.Asp118=
ENST00000585851.2:c.353A=	ENSP00000467912.2:p.Asp118=
ENST00000586243.5:c.527A=	ENSP00000467240.2:p.Asp176=
ENST00000586358.5:n.350A=
ENST00000589152.5:n.617A=
ENST00000591133.2:n.423A=
ENST00000652231.1:c.527A=	ENSP00000498804.1:p.Asp176=
XM_005259617.1:c.527A=	XP_005259674.1:p.Asp176=
XM_005259617.3:c.527A=	XP_005259674.1:p.Asp176=
XM_005259618.3:c.527A=	XP_005259675.1:p.Asp176=
XM_011528209.1:c.305A=	XP_011526511.1:p.Asp102=
XM_011528209.2:c.305A=	XP_011526511.1:p.Asp102=
XR_001753738.2:n.1152A=
XR_001753739.1:n.1152A=
XR_001753740.2:n.1152A=
XR_936204.1:n.1152A=