Canonical Allele Identifier: CA2695227960
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1221270_1221271insA , CM000681.2:g.1221270_1221271insA GRCh38
NC_000019.9:g.1221269_1221270insA , CM000681.1:g.1221269_1221270insA GRCh37
NC_000019.8:g.1172269_1172270insA NCBI36
NG_007460.2:g.36864_36865insA , LRG_319:g.36864_36865insA

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.792_793insA ENSP00000490268.2:p.Glu265ArgfsTer20
ENST00000585748.3:c.420_421insA ENSP00000477641.2:p.Glu141ArgfsTer20
ENST00000585851.2:c.618_619insA ENSP00000467912.2:p.Glu207ArgfsTer20
ENST00000326873.12:c.792_793insA MANE Select ENSP00000324856.6:p.Glu265ArgfsTer20
ENST00000652231.1:c.792_793insA ENSP00000498804.1:p.Glu265ArgfsTer20
ENST00000326873.11:c.792_793insA ENSP00000324856.6:p.Glu265ArgfsTer20
ENST00000586243.5:c.792_793insA ENSP00000467240.2:p.Glu265ArgfsTer20
ENST00000586358.5:n.690_691insA
ENST00000589152.5:n.882_883insA
ENST00000591133.2:n.763_764insA
NM_000455.4:c.792_793insA , LRG_319t1:c.792_793insA NP_000446.1:p.Glu265ArgfsTer20
XM_005259617.1:c.792_793insA XP_005259674.1:p.Glu265ArgfsTer20
XM_005259618.3:c.792_793insA XP_005259675.1:p.Glu265ArgfsTer20
XM_011528209.1:c.570_571insA XP_011526511.1:p.Glu191ArgfsTer20
XR_936204.1:n.1417_1418insA
XM_005259617.3:c.792_793insA XP_005259674.1:p.Glu265ArgfsTer20
XM_011528209.2:c.570_571insA XP_011526511.1:p.Glu191ArgfsTer20
XR_001753738.2:n.1417_1418insA
XR_001753739.1:n.1417_1418insA
XR_001753740.2:n.1417_1418insA
NM_000455.5:c.792_793insA MANE Select NP_000446.1:p.Glu265ArgfsTer20