Canonical Allele Identifier: CA2317593726

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226547G= , CM000681.2:g.1226547G=	GRCh38
NC_000019.9:g.1226546G= , CM000681.1:g.1226546G=	GRCh37
NC_000019.8:g.1177546G=	NCBI36
NG_007460.2:g.42141G= , LRG_319:g.42141G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2803G=	ENSP00000490268.2:n.*2803G=
ENST00000585748.3:c.830G=	ENSP00000477641.2:p.Ser277=
ENST00000585851.2:c.1028G=	ENSP00000467912.2:p.Ser343=
ENST00000326873.12:c.1202G= MANE Select	ENSP00000324856.6:p.Ser401=
ENST00000326873.11:c.1202G=	ENSP00000324856.6:p.Ser401=
ENST00000585465.2:n.2935G=
ENST00000586243.5:c.1202G=	ENSP00000467240.2:p.Ser401=
ENST00000589152.5:n.1900G=
NM_000455.4:c.1202G= , LRG_319t1:c.1202G=	NP_000446.1:p.Ser401=
XM_005259617.1:c.1197G=	XP_005259674.1:p.Glu399=
XM_011528209.1:c.975G=	XP_011526511.1:p.Glu325=
XM_005259617.3:c.1197G=	XP_005259674.1:p.Glu399=
XM_011528209.2:c.975G=	XP_011526511.1:p.Glu325=
XR_001753738.2:n.2008G=
XR_001753740.2:n.1978G=
NM_000455.5:c.1202G= MANE Select	NP_000446.1:p.Ser401=