Canonical Allele Identifier: CA2317593795

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226625T= , CM000681.2:g.1226625T=	GRCh38
NC_000019.9:g.1226624T= , CM000681.1:g.1226624T=	GRCh37
NC_000019.8:g.1177624T=	NCBI36
NG_007460.2:g.42219T= , LRG_319:g.42219T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2881T=	ENSP00000490268.2:n.*2881T=
ENST00000585748.3:c.908T=	ENSP00000477641.2:p.Leu303=
ENST00000585851.2:c.1106T=	ENSP00000467912.2:p.Leu369=
ENST00000326873.12:c.1280T= MANE Select	ENSP00000324856.6:p.Leu427=
ENST00000326873.11:c.1280T=	ENSP00000324856.6:p.Leu427=
ENST00000585465.2:n.3013T=
ENST00000586243.5:c.1277T=	ENSP00000467240.2:p.Leu426=
ENST00000589152.5:n.1978T=
NM_000455.4:c.1280T= , LRG_319t1:c.1280T=	NP_000446.1:p.Leu427=
XM_005259617.1:c.1275T=	XP_005259674.1:p.Ala425=
XM_011528209.1:c.1053T=	XP_011526511.1:p.Ala351=
XM_005259617.3:c.1275T=	XP_005259674.1:p.Ala425=
XM_011528209.2:c.1053T=	XP_011526511.1:p.Ala351=
XR_001753738.2:n.2086T=
XR_001753740.2:n.2056T=
NM_000455.5:c.1280T= MANE Select	NP_000446.1:p.Leu427=