Canonical Allele Identifier: CA2317593803

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226632C= , CM000681.2:g.1226632C=	GRCh38
NC_000019.9:g.1226631C= , CM000681.1:g.1226631C=	GRCh37
NC_000019.8:g.1177631C=	NCBI36
NG_007460.2:g.42226C= , LRG_319:g.42226C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2888C=	ENSP00000490268.2:n.*2888C=
ENST00000585748.3:c.915C=	ENSP00000477641.2:p.Ala305=
ENST00000585851.2:c.1113C=	ENSP00000467912.2:p.Ala371=
ENST00000326873.12:c.1287C= MANE Select	ENSP00000324856.6:p.Ala429=
ENST00000326873.11:c.1287C=	ENSP00000324856.6:p.Ala429=
ENST00000585465.2:n.3020C=
ENST00000586243.5:c.1284C=	ENSP00000467240.2:p.Ala428=
ENST00000589152.5:n.1985C=
NM_000455.4:c.1287C= , LRG_319t1:c.1287C=	NP_000446.1:p.Ala429=
XM_005259617.1:c.1282C=	XP_005259674.1:p.Leu428=
XM_011528209.1:c.1060C=	XP_011526511.1:p.Leu354=
XM_005259617.3:c.1282C=	XP_005259674.1:p.Leu428=
XM_011528209.2:c.1060C=	XP_011526511.1:p.Leu354=
XR_001753738.2:n.2093C=
XR_001753740.2:n.2063C=
NM_000455.5:c.1287C= MANE Select	NP_000446.1:p.Ala429=