Canonical Allele Identifier: CA2317581618

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207027_1207030delinsGCGC , CM000681.2:g.1207027_1207030delinsGCGC	GRCh38
NC_000019.9:g.1207026_1207029delinsGCGC , CM000681.1:g.1207026_1207029delinsGCGC	GRCh37
NC_000019.8:g.1158026_1158029delinsGCGC	NCBI36
NG_007460.2:g.22621_22624delinsGCGC , LRG_319:g.22621_22624delinsGCGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.114_117delinsGCGC	ENSP00000490268.2:p.Pro38=
ENST00000585748.3:c.-82-11390_-82-11387delinsGCGC	ENSP00000477641.2:n.-82-11390_-82-11387de...
ENST00000585851.2:c.114_117delinsGCGC	ENSP00000467912.2:p.Pro38=
ENST00000326873.12:c.114_117delinsGCGC MANE Select	ENSP00000324856.6:p.Pro38=
ENST00000652231.1:c.114_117delinsGCGC	ENSP00000498804.1:p.Pro38=
ENST00000326873.11:c.114_117delinsGCGC	ENSP00000324856.6:p.Pro38=
ENST00000585748.2:c.-82-11390_-82-11387delinsGCGC	ENSP00000477641.1:n.-82-11390_-82-11387de...
ENST00000585851.1:c.114_117delinsGCGC	ENSP00000467912.1:p.Pro38=
ENST00000586243.5:c.114_117delinsGCGC	ENSP00000467240.2:p.Pro38=
ENST00000589152.5:n.204_207delinsGCGC
ENST00000593219.5:c.114_117delinsGCGC	ENSP00000466610.1:p.Pro38=
NM_000455.4:c.114_117delinsGCGC , LRG_319t1:c.114_117delinsGCGC	NP_000446.1:p.Pro38=
XM_005259617.1:c.114_117delinsGCGC	XP_005259674.1:p.Pro38=
XM_005259618.3:c.114_117delinsGCGC	XP_005259675.1:p.Pro38=
XM_011528209.1:c.-240_-237delinsGCGC	XP_011526511.1:n.-240_-237delinsGCGC
XR_936204.1:n.739_742delinsGCGC
XM_005259617.3:c.114_117delinsGCGC	XP_005259674.1:p.Pro38=
XM_011528209.2:c.-240_-237delinsGCGC	XP_011526511.1:n.-240_-237delinsGCGC
XR_001753738.2:n.739_742delinsGCGC
XR_001753739.1:n.739_742delinsGCGC
XR_001753740.2:n.739_742delinsGCGC
NM_000455.5:c.114_117delinsGCGC MANE Select	NP_000446.1:p.Pro38=