Canonical Allele Identifier: CA913190684

Gene: STK11

Linked Data

• ClinVar Variation Id: 619729
• ClinVar RCV Id: RCV000759360
• dbSNP Id: rs1568709203

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221259_1221266dup , CM000681.2:g.1221259_1221266dup	GRCh38
NC_000019.9:g.1221258_1221265dup , CM000681.1:g.1221258_1221265dup	GRCh37
NC_000019.8:g.1172258_1172265dup	NCBI36
NG_007460.2:g.36853_36860dup , LRG_319:g.36853_36860dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.781_788dup	ENSP00000490268.2:p.Leu263PhefsTer27
ENST00000585748.3:c.409_416dup	ENSP00000477641.2:p.Leu139PhefsTer27
ENST00000585851.2:c.607_614dup	ENSP00000467912.2:p.Leu205PhefsTer27
ENST00000326873.12:c.781_788dup MANE Select	ENSP00000324856.6:p.Leu263PhefsTer27
ENST00000652231.1:c.781_788dup	ENSP00000498804.1:p.Leu263PhefsTer27
ENST00000326873.11:c.781_788dup	ENSP00000324856.6:p.Leu263PhefsTer27
ENST00000586243.5:c.781_788dup	ENSP00000467240.2:p.Leu263PhefsTer27
ENST00000586358.5:n.679_686dup
ENST00000589152.5:n.871_878dup
ENST00000591133.2:n.752_759dup
NM_000455.4:c.781_788dup , LRG_319t1:c.781_788dup	NP_000446.1:p.Leu263PhefsTer27
XM_005259617.1:c.781_788dup	XP_005259674.1:p.Leu263PhefsTer27
XM_005259618.3:c.781_788dup	XP_005259675.1:p.Leu263PhefsTer27
XM_011528209.1:c.559_566dup	XP_011526511.1:p.Leu189PhefsTer27
XR_936204.1:n.1406_1413dup
XM_005259617.3:c.781_788dup	XP_005259674.1:p.Leu263PhefsTer27
XM_011528209.2:c.559_566dup	XP_011526511.1:p.Leu189PhefsTer27
XR_001753738.2:n.1406_1413dup
XR_001753739.1:n.1406_1413dup
XR_001753740.2:n.1406_1413dup
NM_000455.5:c.781_788dup MANE Select	NP_000446.1:p.Leu263PhefsTer27