Canonical Allele Identifier: CA2317581679

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207107_1207111delinsAGGTG , CM000681.2:g.1207107_1207111delinsAGGTG	GRCh38
NC_000019.9:g.1207106_1207110delinsAGGTG , CM000681.1:g.1207106_1207110delinsAGGTG	GRCh37
NC_000019.8:g.1158106_1158110delinsAGGTG	NCBI36
NG_007460.2:g.22701_22705delinsAGGTG , LRG_319:g.22701_22705delinsAGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.194_198delinsAGGTG	ENSP00000490268.2:p.Glu65=
ENST00000585748.3:c.-82-11310_-82-11306delinsAGGTG	ENSP00000477641.2:n.-82-11310_-82-11306delinsAGGTG
ENST00000585851.2:c.194_198delinsAGGTG	ENSP00000467912.2:p.Glu65=
ENST00000326873.12:c.194_198delinsAGGTG MANE Select	ENSP00000324856.6:p.Glu65=
ENST00000652231.1:c.194_198delinsAGGTG	ENSP00000498804.1:p.Glu65=
ENST00000326873.11:c.194_198delinsAGGTG	ENSP00000324856.6:p.Glu65=
ENST00000585748.2:c.-82-11310_-82-11306delinsAGGTG	ENSP00000477641.1:n.-82-11310_-82-11306delinsAGGTG
ENST00000585851.1:c.194_198delinsAGGTG	ENSP00000467912.1:p.Glu65=
ENST00000586243.5:c.194_198delinsAGGTG	ENSP00000467240.2:p.Glu65=
ENST00000586358.5:n.17_21delinsAGGTG
ENST00000589152.5:n.284_288delinsAGGTG
ENST00000593219.5:c.194_198delinsAGGTG	ENSP00000466610.1:p.Glu65=
NM_000455.4:c.194_198delinsAGGTG , LRG_319t1:c.194_198delinsAGGTG	NP_000446.1:p.Glu65=
XM_005259617.1:c.194_198delinsAGGTG	XP_005259674.1:p.Glu65=
XM_005259618.3:c.194_198delinsAGGTG	XP_005259675.1:p.Glu65=
XM_011528209.1:c.-160_-156delinsAGGTG	XP_011526511.1:n.-160_-156delinsAGGTG
XR_936204.1:n.819_823delinsAGGTG
XM_005259617.3:c.194_198delinsAGGTG	XP_005259674.1:p.Glu65=
XM_011528209.2:c.-160_-156delinsAGGTG	XP_011526511.1:n.-160_-156delinsAGGTG
XR_001753738.2:n.819_823delinsAGGTG
XR_001753739.1:n.819_823delinsAGGTG
XR_001753740.2:n.819_823delinsAGGTG
NM_000455.5:c.194_198delinsAGGTG MANE Select	NP_000446.1:p.Glu65=