Canonical Allele Identifier: CA2317589116

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219398T= , CM000681.2:g.1219398T=	GRCh38
NC_000019.9:g.1219397T= , CM000681.1:g.1219397T=	GRCh37
NC_000019.8:g.1170397T=	NCBI36
NG_007460.2:g.34992T= , LRG_319:g.34992T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.449T=	ENSP00000490268.2:p.Val150=
ENST00000585748.3:c.77T=	ENSP00000477641.2:p.Val26=
ENST00000585851.2:c.291-975T=	ENSP00000467912.2:n.291-975T=
ENST00000326873.12:c.449T= MANE Select	ENSP00000324856.6:p.Val150=
ENST00000652231.1:c.449T=	ENSP00000498804.1:p.Val150=
ENST00000326873.11:c.449T=	ENSP00000324856.6:p.Val150=
ENST00000585851.1:c.291-975T=	ENSP00000467912.1:n.291-975T=
ENST00000586243.5:c.449T=	ENSP00000467240.2:p.Val150=
ENST00000586358.5:n.272T=
ENST00000589152.5:n.539T=
NM_000455.4:c.449T= , LRG_319t1:c.449T=	NP_000446.1:p.Val150=
XM_005259617.1:c.449T=	XP_005259674.1:p.Val150=
XM_005259618.3:c.449T=	XP_005259675.1:p.Val150=
XM_011528209.1:c.227T=	XP_011526511.1:p.Val76=
XR_936204.1:n.1074T=
XM_005259617.3:c.449T=	XP_005259674.1:p.Val150=
XM_011528209.2:c.227T=	XP_011526511.1:p.Val76=
XR_001753738.2:n.1074T=
XR_001753739.1:n.1074T=
XR_001753740.2:n.1074T=
NM_000455.5:c.449T= MANE Select	NP_000446.1:p.Val150=