Canonical Allele Identifier: CA2317593664

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226476C= , CM000681.2:g.1226476C=	GRCh38
NC_000019.9:g.1226475C= , CM000681.1:g.1226475C=	GRCh37
NC_000019.8:g.1177475C=	NCBI36
NG_007460.2:g.42070C= , LRG_319:g.42070C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2732C=	ENSP00000490268.2:n.*2732C=
ENST00000585748.3:c.759C=	ENSP00000477641.2:p.Ala253=
ENST00000585851.2:c.957C=	ENSP00000467912.2:p.Ala319=
ENST00000326873.12:c.1131C= MANE Select	ENSP00000324856.6:p.Ala377=
ENST00000326873.11:c.1131C=	ENSP00000324856.6:p.Ala377=
ENST00000585465.2:n.2864C=
ENST00000586243.5:c.1131C=	ENSP00000467240.2:p.Ala377=
ENST00000589152.5:n.1829C=
NM_000455.4:c.1131C= , LRG_319t1:c.1131C=	NP_000446.1:p.Ala377=
XM_005259617.1:c.1126C=	XP_005259674.1:p.Gln376=
XM_011528209.1:c.904C=	XP_011526511.1:p.Gln302=
XM_005259617.3:c.1126C=	XP_005259674.1:p.Gln376=
XM_011528209.2:c.904C=	XP_011526511.1:p.Gln302=
XR_001753738.2:n.1937C=
XR_001753740.2:n.1907C=
NM_000455.5:c.1131C= MANE Select	NP_000446.1:p.Ala377=