Canonical Allele Identifier: CA2317593796

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226626G= , CM000681.2:g.1226626G=	GRCh38
NC_000019.9:g.1226625G= , CM000681.1:g.1226625G=	GRCh37
NC_000019.8:g.1177625G=	NCBI36
NG_007460.2:g.42220G= , LRG_319:g.42220G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2882G=	ENSP00000490268.2:n.*2882G=
ENST00000585748.3:c.909G=	ENSP00000477641.2:p.Leu303=
ENST00000585851.2:c.1107G=	ENSP00000467912.2:p.Leu369=
ENST00000326873.12:c.1281G= MANE Select	ENSP00000324856.6:p.Leu427=
ENST00000326873.11:c.1281G=	ENSP00000324856.6:p.Leu427=
ENST00000585465.2:n.3014G=
ENST00000586243.5:c.1278G=	ENSP00000467240.2:p.Leu426=
ENST00000589152.5:n.1979G=
NM_000455.4:c.1281G= , LRG_319t1:c.1281G=	NP_000446.1:p.Leu427=
XM_005259617.1:c.1276G=	XP_005259674.1:p.Val426=
XM_011528209.1:c.1054G=	XP_011526511.1:p.Val352=
XM_005259617.3:c.1276G=	XP_005259674.1:p.Val426=
XM_011528209.2:c.1054G=	XP_011526511.1:p.Val352=
XR_001753738.2:n.2087G=
XR_001753740.2:n.2057G=
NM_000455.5:c.1281G= MANE Select	NP_000446.1:p.Leu427=