Canonical Allele Identifier: CA2813238394

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207343_1207344insT , CM000681.2:g.1207343_1207344insT	GRCh38
NC_000019.9:g.1207342_1207343insT , CM000681.1:g.1207342_1207343insT	GRCh37
NC_000019.8:g.1158342_1158343insT	NCBI36
NG_007460.2:g.22937_22938insT , LRG_319:g.22937_22938insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.290+140_290+141insT	ENSP00000490268.2:n.290+140_290+141insT
ENST00000585748.3:c.-82-11074_-82-11073insT	ENSP00000477641.2:n.-82-11074_-82-11073insT
ENST00000585851.2:c.290+140_290+141insT	ENSP00000467912.2:n.290+140_290+141insT
ENST00000326873.12:c.290+140_290+141insT MANE Select	ENSP00000324856.6:n.290+140_290+141insT
ENST00000652231.1:c.290+140_290+141insT	ENSP00000498804.1:n.290+140_290+141insT
ENST00000326873.11:c.290+140_290+141insT	ENSP00000324856.6:n.290+140_290+141insT
ENST00000585748.2:c.-82-11074_-82-11073insT	ENSP00000477641.1:n.-82-11074_-82-11073insT
ENST00000585851.1:c.290+140_290+141insT	ENSP00000467912.1:n.290+140_290+141insT
ENST00000586243.5:c.290+140_290+141insT	ENSP00000467240.2:n.290+140_290+141insT
ENST00000586358.5:n.113+140_113+141insT
ENST00000589152.5:n.380+140_380+141insT
ENST00000593219.5:c.290+140_290+141insT	ENSP00000466610.1:n.290+140_290+141insT
NM_000455.4:c.290+140_290+141insT , LRG_319t1:c.290+140_290+141insT	NP_000446.1:n.290+140_290+141insT
XM_005259617.1:c.290+140_290+141insT	XP_005259674.1:n.290+140_290+141insT
XM_005259618.3:c.290+140_290+141insT	XP_005259675.1:n.290+140_290+141insT
XM_011528209.1:c.-64+140_-64+141insT	XP_011526511.1:n.-64+140_-64+141insT
XR_936204.1:n.915+140_915+141insT
XM_005259617.3:c.290+140_290+141insT	XP_005259674.1:n.290+140_290+141insT
XM_011528209.2:c.-64+140_-64+141insT	XP_011526511.1:n.-64+140_-64+141insT
XR_001753738.2:n.915+140_915+141insT
XR_001753739.1:n.915+140_915+141insT
XR_001753740.2:n.915+140_915+141insT
NM_000455.5:c.290+140_290+141insT MANE Select	NP_000446.1:n.290+140_290+141insT