Canonical Allele Identifier: CA2317588572

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218500T= , CM000681.2:g.1218500T=	GRCh38
NC_000019.9:g.1218499T= , CM000681.1:g.1218499T=	GRCh37
NC_000019.8:g.1169499T=	NCBI36
NG_007460.2:g.34094T= , LRG_319:g.34094T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.374T=	ENSP00000490268.2:p.Met125=
ENST00000585748.3:c.2T=	ENSP00000477641.2:p.Met1=
ENST00000585851.2:c.291-1873T=	ENSP00000467912.2:n.291-1873T=
ENST00000326873.12:c.374T= MANE Select	ENSP00000324856.6:p.Met125=
ENST00000652231.1:c.374T=	ENSP00000498804.1:p.Met125=
ENST00000326873.11:c.374T=	ENSP00000324856.6:p.Met125=
ENST00000585748.2:c.2T=	ENSP00000477641.1:p.Met1=
ENST00000585851.1:c.291-1873T=	ENSP00000467912.1:n.291-1873T=
ENST00000586243.5:c.374T=	ENSP00000467240.2:p.Met125=
ENST00000586358.5:n.197T=
ENST00000589152.5:n.464T=
ENST00000593219.5:c.*199T=	ENSP00000466610.1:n.*199T=
NM_000455.4:c.374T= , LRG_319t1:c.374T=	NP_000446.1:p.Met125=
XM_005259617.1:c.374T=	XP_005259674.1:p.Met125=
XM_005259618.3:c.374T=	XP_005259675.1:p.Met125=
XM_011528209.1:c.152T=	XP_011526511.1:p.Met51=
XR_936204.1:n.999T=
XM_005259617.3:c.374T=	XP_005259674.1:p.Met125=
XM_011528209.2:c.152T=	XP_011526511.1:p.Met51=
XR_001753738.2:n.999T=
XR_001753739.1:n.999T=
XR_001753740.2:n.999T=
NM_000455.5:c.374T= MANE Select	NP_000446.1:p.Met125=