Canonical Allele Identifier: CA2317593718

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226539G= , CM000681.2:g.1226539G=	GRCh38
NC_000019.9:g.1226538G= , CM000681.1:g.1226538G=	GRCh37
NC_000019.8:g.1177538G=	NCBI36
NG_007460.2:g.42133G= , LRG_319:g.42133G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2795G=	ENSP00000490268.2:n.*2795G=
ENST00000585748.3:c.822G=	ENSP00000477641.2:p.Ala274=
ENST00000585851.2:c.1020G=	ENSP00000467912.2:p.Ala340=
ENST00000326873.12:c.1194G= MANE Select	ENSP00000324856.6:p.Ala398=
ENST00000326873.11:c.1194G=	ENSP00000324856.6:p.Ala398=
ENST00000585465.2:n.2927G=
ENST00000586243.5:c.1194G=	ENSP00000467240.2:p.Ala398=
ENST00000589152.5:n.1892G=
NM_000455.4:c.1194G= , LRG_319t1:c.1194G=	NP_000446.1:p.Ala398=
XM_005259617.1:c.1189G=	XP_005259674.1:p.Ala397=
XM_011528209.1:c.967G=	XP_011526511.1:p.Ala323=
XM_005259617.3:c.1189G=	XP_005259674.1:p.Ala397=
XM_011528209.2:c.967G=	XP_011526511.1:p.Ala323=
XR_001753738.2:n.2000G=
XR_001753740.2:n.1970G=
NM_000455.5:c.1194G= MANE Select	NP_000446.1:p.Ala398=