Canonical Allele Identifier: CA2317593798

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226628C= , CM000681.2:g.1226628C=	GRCh38
NC_000019.9:g.1226627C= , CM000681.1:g.1226627C=	GRCh37
NC_000019.8:g.1177627C=	NCBI36
NG_007460.2:g.42222C= , LRG_319:g.42222C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2884C=	ENSP00000490268.2:n.*2884C=
ENST00000585748.3:c.911C=	ENSP00000477641.2:p.Ser304=
ENST00000585851.2:c.1109C=	ENSP00000467912.2:p.Ser370=
ENST00000326873.12:c.1283C= MANE Select	ENSP00000324856.6:p.Ser428=
ENST00000326873.11:c.1283C=	ENSP00000324856.6:p.Ser428=
ENST00000585465.2:n.3016C=
ENST00000586243.5:c.1280C=	ENSP00000467240.2:p.Ser427=
ENST00000589152.5:n.1981C=
NM_000455.4:c.1283C= , LRG_319t1:c.1283C=	NP_000446.1:p.Ser428=
XM_005259617.1:c.1278C=	XP_005259674.1:p.Val426=
XM_011528209.1:c.1056C=	XP_011526511.1:p.Val352=
XM_005259617.3:c.1278C=	XP_005259674.1:p.Val426=
XM_011528209.2:c.1056C=	XP_011526511.1:p.Val352=
XR_001753738.2:n.2089C=
XR_001753740.2:n.2059C=
NM_000455.5:c.1283C= MANE Select	NP_000446.1:p.Ser428=