Canonical Allele Identifier: CA2317593680

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226495C= , CM000681.2:g.1226495C=	GRCh38
NC_000019.9:g.1226494C= , CM000681.1:g.1226494C=	GRCh37
NC_000019.8:g.1177494C=	NCBI36
NG_007460.2:g.42089C= , LRG_319:g.42089C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2751C=	ENSP00000490268.2:n.*2751C=
ENST00000585748.3:c.778C=	ENSP00000477641.2:p.Arg260=
ENST00000585851.2:c.976C=	ENSP00000467912.2:p.Arg326=
ENST00000326873.12:c.1150C= MANE Select	ENSP00000324856.6:p.Arg384=
ENST00000326873.11:c.1150C=	ENSP00000324856.6:p.Arg384=
ENST00000585465.2:n.2883C=
ENST00000586243.5:c.1150C=	ENSP00000467240.2:p.Arg384=
ENST00000589152.5:n.1848C=
NM_000455.4:c.1150C= , LRG_319t1:c.1150C=	NP_000446.1:p.Arg384=
XM_005259617.1:c.1145C=	XP_005259674.1:p.Pro382=
XM_011528209.1:c.923C=	XP_011526511.1:p.Pro308=
XM_005259617.3:c.1145C=	XP_005259674.1:p.Pro382=
XM_011528209.2:c.923C=	XP_011526511.1:p.Pro308=
XR_001753738.2:n.1956C=
XR_001753740.2:n.1926C=
NM_000455.5:c.1150C= MANE Select	NP_000446.1:p.Arg384=