Canonical Allele Identifier: CA2317591548

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223120C= , CM000681.2:g.1223120C=	GRCh38
NC_000019.9:g.1223119C= , CM000681.1:g.1223119C=	GRCh37
NC_000019.8:g.1174119C=	NCBI36
NG_007460.2:g.38714C= , LRG_319:g.38714C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1056C=	ENSP00000490268.2:p.Asp352=
ENST00000585748.3:c.684C=	ENSP00000477641.2:p.Asp228=
ENST00000585851.2:c.882C=	ENSP00000467912.2:p.Asp294=
ENST00000326873.12:c.1056C= MANE Select	ENSP00000324856.6:p.Asp352=
ENST00000652231.1:c.1056C=	ENSP00000498804.1:p.Asp352=
ENST00000326873.11:c.1056C=	ENSP00000324856.6:p.Asp352=
ENST00000586243.5:c.1056C=	ENSP00000467240.2:p.Asp352=
ENST00000589152.5:n.1754C=
NM_000455.4:c.1056C= , LRG_319t1:c.1056C=	NP_000446.1:p.Asp352=
XM_005259617.1:c.1056C=	XP_005259674.1:p.Asp352=
XM_005259618.3:c.1056C=	XP_005259675.1:p.Asp352=
XM_011528209.1:c.834C=	XP_011526511.1:p.Asp278=
XR_936204.1:n.1832C=
XM_005259617.3:c.1056C=	XP_005259674.1:p.Asp352=
XM_011528209.2:c.834C=	XP_011526511.1:p.Asp278=
XR_001753738.2:n.1862C=
XR_001753739.1:n.1862C=
XR_001753740.2:n.1832C=
NM_000455.5:c.1056C= MANE Select	NP_000446.1:p.Asp352=