Canonical Allele Identifier: CA2317593752

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226578C= , CM000681.2:g.1226578C=	GRCh38
NC_000019.9:g.1226577C= , CM000681.1:g.1226577C=	GRCh37
NC_000019.8:g.1177577C=	NCBI36
NG_007460.2:g.42172C= , LRG_319:g.42172C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2834C=	ENSP00000490268.2:n.*2834C=
ENST00000585748.3:c.861C=	ENSP00000477641.2:p.Pro287=
ENST00000585851.2:c.1059C=	ENSP00000467912.2:p.Pro353=
ENST00000326873.12:c.1233C= MANE Select	ENSP00000324856.6:p.Pro411=
ENST00000326873.11:c.1233C=	ENSP00000324856.6:p.Pro411=
ENST00000585465.2:n.2966C=
ENST00000586243.5:c.1232C=	ENSP00000467240.2:p.Pro411=
ENST00000589152.5:n.1931C=
NM_000455.4:c.1233C= , LRG_319t1:c.1233C=	NP_000446.1:p.Pro411=
XM_005259617.1:c.1228C=	XP_005259674.1:p.Gln410=
XM_011528209.1:c.1006C=	XP_011526511.1:p.Gln336=
XM_005259617.3:c.1228C=	XP_005259674.1:p.Gln410=
XM_011528209.2:c.1006C=	XP_011526511.1:p.Gln336=
XR_001753738.2:n.2039C=
XR_001753740.2:n.2009C=
NM_000455.5:c.1233C= MANE Select	NP_000446.1:p.Pro411=