Canonical Allele Identifier: CA2579985610

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220401_1220409del , CM000681.2:g.1220401_1220409del	GRCh38
NC_000019.9:g.1220400_1220408del , CM000681.1:g.1220400_1220408del	GRCh37
NC_000019.8:g.1171400_1171408del	NCBI36
NG_007460.2:g.35995_36003del , LRG_319:g.35995_36003del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.493_501del	ENSP00000490268.2:p.Glu165_Leu167del
ENST00000585748.3:c.121_129del	ENSP00000477641.2:p.Glu41_Leu43del
ENST00000585851.2:c.319_327del	ENSP00000467912.2:p.Glu107_Leu109del
ENST00000326873.12:c.493_501del MANE Select	ENSP00000324856.6:p.Glu165_Leu167del
ENST00000652231.1:c.493_501del	ENSP00000498804.1:p.Glu165_Leu167del
ENST00000326873.11:c.493_501del	ENSP00000324856.6:p.Glu165_Leu167del
ENST00000585851.1:c.319_327del	ENSP00000467912.1:p.Glu107_Leu109del
ENST00000586243.5:c.493_501del	ENSP00000467240.2:p.Glu165_Leu167del
ENST00000586358.5:n.316_324del
ENST00000589152.5:n.583_591del
ENST00000591133.2:n.389_397del
NM_000455.4:c.493_501del , LRG_319t1:c.493_501del	NP_000446.1:p.Glu165_Leu167del
XM_005259617.1:c.493_501del	XP_005259674.1:p.Glu165_Leu167del
XM_005259618.3:c.493_501del	XP_005259675.1:p.Glu165_Leu167del
XM_011528209.1:c.271_279del	XP_011526511.1:p.Glu91_Leu93del
XR_936204.1:n.1118_1126del
XM_005259617.3:c.493_501del	XP_005259674.1:p.Glu165_Leu167del
XM_011528209.2:c.271_279del	XP_011526511.1:p.Glu91_Leu93del
XR_001753738.2:n.1118_1126del
XR_001753739.1:n.1118_1126del
XR_001753740.2:n.1118_1126del
NM_000455.5:c.493_501del MANE Select	NP_000446.1:p.Glu165_Leu167del