Canonical Allele Identifier: CA2580610739

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218475_1218489del , CM000681.2:g.1218475_1218489del	GRCh38
NC_000019.9:g.1218474_1218488del , CM000681.1:g.1218474_1218488del	GRCh37
NC_000019.8:g.1169474_1169488del	NCBI36
NG_007460.2:g.34069_34083del , LRG_319:g.34069_34083del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.349_363del	ENSP00000490268.2:p.Leu117_Glu121del
ENST00000585748.3:c.-24_-10del	ENSP00000477641.2:n.-24_-10del
ENST00000585851.2:c.291-1898_291-1884del	ENSP00000467912.2:n.291-1898_291-1884del
ENST00000326873.12:c.349_363del MANE Select	ENSP00000324856.6:p.Leu117_Glu121del
ENST00000652231.1:c.349_363del	ENSP00000498804.1:p.Leu117_Glu121del
ENST00000326873.11:c.349_363del	ENSP00000324856.6:p.Leu117_Glu121del
ENST00000585748.2:c.-24_-10del	ENSP00000477641.1:n.-24_-10del
ENST00000585851.1:c.291-1898_291-1884del	ENSP00000467912.1:n.291-1898_291-1884del
ENST00000586243.5:c.349_363del	ENSP00000467240.2:p.Leu117_Glu121del
ENST00000586358.5:n.172_186del
ENST00000589152.5:n.439_453del
ENST00000593219.5:c.*174_*188del	ENSP00000466610.1:n.*174_*188del
NM_000455.4:c.349_363del , LRG_319t1:c.349_363del	NP_000446.1:p.Leu117_Glu121del
XM_005259617.1:c.349_363del	XP_005259674.1:p.Leu117_Glu121del
XM_005259618.3:c.349_363del	XP_005259675.1:p.Leu117_Glu121del
XM_011528209.1:c.127_141del	XP_011526511.1:p.Leu43_Glu47del
XR_936204.1:n.974_988del
XM_005259617.3:c.349_363del	XP_005259674.1:p.Leu117_Glu121del
XM_011528209.2:c.127_141del	XP_011526511.1:p.Leu43_Glu47del
XR_001753738.2:n.974_988del
XR_001753739.1:n.974_988del
XR_001753740.2:n.974_988del
NM_000455.5:c.349_363del MANE Select	NP_000446.1:p.Leu117_Glu121del