Canonical Allele Identifier: CA2317590332

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221263_1221266delinsAGTT , CM000681.2:g.1221263_1221266delinsAGTT	GRCh38
NC_000019.9:g.1221262_1221265delinsAGTT , CM000681.1:g.1221262_1221265delinsAGTT	GRCh37
NC_000019.8:g.1172262_1172265delinsAGTT	NCBI36
NG_007460.2:g.36857_36860delinsAGTT , LRG_319:g.36857_36860delinsAGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.785_788delinsAGTT	ENSP00000490268.2:p.Lys262=
ENST00000585748.3:c.413_416delinsAGTT	ENSP00000477641.2:p.Lys138=
ENST00000585851.2:c.611_614delinsAGTT	ENSP00000467912.2:p.Lys204=
ENST00000326873.12:c.785_788delinsAGTT MANE Select	ENSP00000324856.6:p.Lys262=
ENST00000652231.1:c.785_788delinsAGTT	ENSP00000498804.1:p.Lys262=
ENST00000326873.11:c.785_788delinsAGTT	ENSP00000324856.6:p.Lys262=
ENST00000586243.5:c.785_788delinsAGTT	ENSP00000467240.2:p.Lys262=
ENST00000586358.5:n.683_686delinsAGTT
ENST00000589152.5:n.875_878delinsAGTT
ENST00000591133.2:n.756_759delinsAGTT
NM_000455.4:c.785_788delinsAGTT , LRG_319t1:c.785_788delinsAGTT	NP_000446.1:p.Lys262=
XM_005259617.1:c.785_788delinsAGTT	XP_005259674.1:p.Lys262=
XM_005259618.3:c.785_788delinsAGTT	XP_005259675.1:p.Lys262=
XM_011528209.1:c.563_566delinsAGTT	XP_011526511.1:p.Lys188=
XR_936204.1:n.1410_1413delinsAGTT
XM_005259617.3:c.785_788delinsAGTT	XP_005259674.1:p.Lys262=
XM_011528209.2:c.563_566delinsAGTT	XP_011526511.1:p.Lys188=
XR_001753738.2:n.1410_1413delinsAGTT
XR_001753739.1:n.1410_1413delinsAGTT
XR_001753740.2:n.1410_1413delinsAGTT
NM_000455.5:c.785_788delinsAGTT MANE Select	NP_000446.1:p.Lys262=