Canonical Allele Identifier: CA2317581533

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206918_1206921delinsAGGT , CM000681.2:g.1206918_1206921delinsAGGT	GRCh38
NC_000019.9:g.1206917_1206920delinsAGGT , CM000681.1:g.1206917_1206920delinsAGGT	GRCh37
NC_000019.8:g.1157917_1157920delinsAGGT	NCBI36
NG_007460.2:g.22512_22515delinsAGGT , LRG_319:g.22512_22515delinsAGGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.5_8delinsAGGT	ENSP00000490268.2:p.Glu2=
ENST00000585748.3:c.-82-11499_-82-11496delinsAGGT	ENSP00000477641.2:n.-82-11499_-82-11496de...
ENST00000585851.2:c.5_8delinsAGGT	ENSP00000467912.2:p.Glu2=
ENST00000326873.12:c.5_8delinsAGGT MANE Select	ENSP00000324856.6:p.Glu2=
ENST00000652231.1:c.5_8delinsAGGT	ENSP00000498804.1:p.Glu2=
ENST00000326873.11:c.5_8delinsAGGT	ENSP00000324856.6:p.Glu2=
ENST00000585748.2:c.-82-11499_-82-11496delinsAGGT	ENSP00000477641.1:n.-82-11499_-82-11496de...
ENST00000585851.1:c.5_8delinsAGGT	ENSP00000467912.1:p.Glu2=
ENST00000586243.5:c.5_8delinsAGGT	ENSP00000467240.2:p.Glu2=
ENST00000589152.5:n.95_98delinsAGGT
ENST00000593219.5:c.5_8delinsAGGT	ENSP00000466610.1:p.Glu2=
NM_000455.4:c.5_8delinsAGGT , LRG_319t1:c.5_8delinsAGGT	NP_000446.1:p.Glu2=
XM_005259617.1:c.5_8delinsAGGT	XP_005259674.1:p.Glu2=
XM_005259618.3:c.5_8delinsAGGT	XP_005259675.1:p.Glu2=
XM_011528209.1:c.-349_-346delinsAGGT	XP_011526511.1:n.-349_-346delinsAGGT
XR_936204.1:n.630_633delinsAGGT
XM_005259617.3:c.5_8delinsAGGT	XP_005259674.1:p.Glu2=
XM_011528209.2:c.-349_-346delinsAGGT	XP_011526511.1:n.-349_-346delinsAGGT
XR_001753738.2:n.630_633delinsAGGT
XR_001753739.1:n.630_633delinsAGGT
XR_001753740.2:n.630_633delinsAGGT
NM_000455.5:c.5_8delinsAGGT MANE Select	NP_000446.1:p.Glu2=