Canonical Allele Identifier: CA2695227874

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219375_1219397del , CM000681.2:g.1219375_1219397del	GRCh38
NC_000019.9:g.1219374_1219396del , CM000681.1:g.1219374_1219396del	GRCh37
NC_000019.8:g.1170374_1170396del	NCBI36
NG_007460.2:g.34969_34991del , LRG_319:g.34969_34991del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.426_448del	ENSP00000490268.2:p.Glu145GlyfsTer10
ENST00000585748.3:c.54_76del	ENSP00000477641.2:p.Glu21GlyfsTer10
ENST00000585851.2:c.291-998_291-976del	ENSP00000467912.2:n.291-998_291-976del
ENST00000326873.12:c.426_448del MANE Select	ENSP00000324856.6:p.Glu145GlyfsTer10
ENST00000652231.1:c.426_448del	ENSP00000498804.1:p.Glu145GlyfsTer10
ENST00000326873.11:c.426_448del	ENSP00000324856.6:p.Glu145GlyfsTer10
ENST00000585851.1:c.291-998_291-976del	ENSP00000467912.1:n.291-998_291-976del
ENST00000586243.5:c.426_448del	ENSP00000467240.2:p.Glu145GlyfsTer10
ENST00000586358.5:n.249_271del
ENST00000589152.5:n.516_538del
NM_000455.4:c.426_448del , LRG_319t1:c.426_448del	NP_000446.1:p.Glu145GlyfsTer10
XM_005259617.1:c.426_448del	XP_005259674.1:p.Glu145GlyfsTer10
XM_005259618.3:c.426_448del	XP_005259675.1:p.Glu145GlyfsTer10
XM_011528209.1:c.204_226del	XP_011526511.1:p.Glu71GlyfsTer10
XR_936204.1:n.1051_1073del
XM_005259617.3:c.426_448del	XP_005259674.1:p.Glu145GlyfsTer10
XM_011528209.2:c.204_226del	XP_011526511.1:p.Glu71GlyfsTer10
XR_001753738.2:n.1051_1073del
XR_001753739.1:n.1051_1073del
XR_001753740.2:n.1051_1073del
NM_000455.5:c.426_448del MANE Select	NP_000446.1:p.Glu145GlyfsTer10