Canonical Allele Identifier: CA2317593779

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226606A= , CM000681.2:g.1226606A=	GRCh38
NC_000019.9:g.1226605A= , CM000681.1:g.1226605A=	GRCh37
NC_000019.8:g.1177605A=	NCBI36
NG_007460.2:g.42200A= , LRG_319:g.42200A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2862A=	ENSP00000490268.2:n.*2862A=
ENST00000585748.3:c.889A=	ENSP00000477641.2:p.Ser297=
ENST00000585851.2:c.1087A=	ENSP00000467912.2:p.Ser363=
ENST00000326873.12:c.1261A= MANE Select	ENSP00000324856.6:p.Ser421=
ENST00000326873.11:c.1261A=	ENSP00000324856.6:p.Ser421=
ENST00000585465.2:n.2994A=
ENST00000586243.5:c.1258A=	ENSP00000467240.2:p.Ser420=
ENST00000589152.5:n.1959A=
NM_000455.4:c.1261A= , LRG_319t1:c.1261A=	NP_000446.1:p.Ser421=
XM_005259617.1:c.1256A=	XP_005259674.1:p.Gln419=
XM_011528209.1:c.1034A=	XP_011526511.1:p.Gln345=
XM_005259617.3:c.1256A=	XP_005259674.1:p.Gln419=
XM_011528209.2:c.1034A=	XP_011526511.1:p.Gln345=
XR_001753738.2:n.2067A=
XR_001753740.2:n.2037A=
NM_000455.5:c.1261A= MANE Select	NP_000446.1:p.Ser421=