Canonical Allele Identifier: CA2317593801

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226630G= , CM000681.2:g.1226630G=	GRCh38
NC_000019.9:g.1226629G= , CM000681.1:g.1226629G=	GRCh37
NC_000019.8:g.1177629G=	NCBI36
NG_007460.2:g.42224G= , LRG_319:g.42224G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2886G=	ENSP00000490268.2:n.*2886G=
ENST00000585748.3:c.913G=	ENSP00000477641.2:p.Ala305=
ENST00000585851.2:c.1111G=	ENSP00000467912.2:p.Ala371=
ENST00000326873.12:c.1285G= MANE Select	ENSP00000324856.6:p.Ala429=
ENST00000326873.11:c.1285G=	ENSP00000324856.6:p.Ala429=
ENST00000585465.2:n.3018G=
ENST00000586243.5:c.1282G=	ENSP00000467240.2:p.Ala428=
ENST00000589152.5:n.1983G=
NM_000455.4:c.1285G= , LRG_319t1:c.1285G=	NP_000446.1:p.Ala429=
XM_005259617.1:c.1280G=	XP_005259674.1:p.Gly427=
XM_011528209.1:c.1058G=	XP_011526511.1:p.Gly353=
XM_005259617.3:c.1280G=	XP_005259674.1:p.Gly427=
XM_011528209.2:c.1058G=	XP_011526511.1:p.Gly353=
XR_001753738.2:n.2091G=
XR_001753740.2:n.2061G=
NM_000455.5:c.1285G= MANE Select	NP_000446.1:p.Ala429=