Canonical Allele Identifier: CA2317593650

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226462C= , CM000681.2:g.1226462C=	GRCh38
NC_000019.9:g.1226461C= , CM000681.1:g.1226461C=	GRCh37
NC_000019.8:g.1177461C=	NCBI36
NG_007460.2:g.42056C= , LRG_319:g.42056C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2718C=	ENSP00000490268.2:n.*2718C=
ENST00000585748.3:c.745C=	ENSP00000477641.2:p.Pro249=
ENST00000585851.2:c.943C=	ENSP00000467912.2:p.Pro315=
ENST00000326873.12:c.1117C= MANE Select	ENSP00000324856.6:p.Pro373=
ENST00000326873.11:c.1117C=	ENSP00000324856.6:p.Pro373=
ENST00000585465.2:n.2850C=
ENST00000586243.5:c.1117C=	ENSP00000467240.2:p.Pro373=
ENST00000589152.5:n.1815C=
NM_000455.4:c.1117C= , LRG_319t1:c.1117C=	NP_000446.1:p.Pro373=
XM_005259617.1:c.1112C=	XP_005259674.1:p.Pro371=
XM_011528209.1:c.890C=	XP_011526511.1:p.Pro297=
XM_005259617.3:c.1112C=	XP_005259674.1:p.Pro371=
XM_011528209.2:c.890C=	XP_011526511.1:p.Pro297=
XR_001753738.2:n.1923C=
XR_001753740.2:n.1893C=
NM_000455.5:c.1117C= MANE Select	NP_000446.1:p.Pro373=