Canonical Allele Identifier: CA2317588567

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218492G= , CM000681.2:g.1218492G=	GRCh38
NC_000019.9:g.1218491G= , CM000681.1:g.1218491G=	GRCh37
NC_000019.8:g.1169491G=	NCBI36
NG_007460.2:g.34086G= , LRG_319:g.34086G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.366G=	ENSP00000490268.2:p.Lys122=
ENST00000585748.3:c.-7G=	ENSP00000477641.2:n.-7G=
ENST00000585851.2:c.291-1881G=	ENSP00000467912.2:n.291-1881G=
ENST00000326873.12:c.366G= MANE Select	ENSP00000324856.6:p.Lys122=
ENST00000652231.1:c.366G=	ENSP00000498804.1:p.Lys122=
ENST00000326873.11:c.366G=	ENSP00000324856.6:p.Lys122=
ENST00000585748.2:c.-7G=	ENSP00000477641.1:n.-7G=
ENST00000585851.1:c.291-1881G=	ENSP00000467912.1:n.291-1881G=
ENST00000586243.5:c.366G=	ENSP00000467240.2:p.Lys122=
ENST00000586358.5:n.189G=
ENST00000589152.5:n.456G=
ENST00000593219.5:c.*191G=	ENSP00000466610.1:n.*191G=
NM_000455.4:c.366G= , LRG_319t1:c.366G=	NP_000446.1:p.Lys122=
XM_005259617.1:c.366G=	XP_005259674.1:p.Lys122=
XM_005259618.3:c.366G=	XP_005259675.1:p.Lys122=
XM_011528209.1:c.144G=	XP_011526511.1:p.Lys48=
XR_936204.1:n.991G=
XM_005259617.3:c.366G=	XP_005259674.1:p.Lys122=
XM_011528209.2:c.144G=	XP_011526511.1:p.Lys48=
XR_001753738.2:n.991G=
XR_001753739.1:n.991G=
XR_001753740.2:n.991G=
NM_000455.5:c.366G= MANE Select	NP_000446.1:p.Lys122=