Canonical Allele Identifier: CA2576546258

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207262_1207263insA , CM000681.2:g.1207262_1207263insA	GRCh38
NC_000019.9:g.1207261_1207262insA , CM000681.1:g.1207261_1207262insA	GRCh37
NC_000019.8:g.1158261_1158262insA	NCBI36
NG_007460.2:g.22856_22857insA , LRG_319:g.22856_22857insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.290+59_290+60insA	ENSP00000490268.2:n.290+59_290+60insA
ENST00000585748.3:c.-82-11155_-82-11154insA	ENSP00000477641.2:n.-82-11155_-82-11154insA
ENST00000585851.2:c.290+59_290+60insA	ENSP00000467912.2:n.290+59_290+60insA
ENST00000326873.12:c.290+59_290+60insA MANE Select	ENSP00000324856.6:n.290+59_290+60insA
ENST00000652231.1:c.290+59_290+60insA	ENSP00000498804.1:n.290+59_290+60insA
ENST00000326873.11:c.290+59_290+60insA	ENSP00000324856.6:n.290+59_290+60insA
ENST00000585748.2:c.-82-11155_-82-11154insA	ENSP00000477641.1:n.-82-11155_-82-11154insA
ENST00000585851.1:c.290+59_290+60insA	ENSP00000467912.1:n.290+59_290+60insA
ENST00000586243.5:c.290+59_290+60insA	ENSP00000467240.2:n.290+59_290+60insA
ENST00000586358.5:n.113+59_113+60insA
ENST00000589152.5:n.380+59_380+60insA
ENST00000593219.5:c.290+59_290+60insA	ENSP00000466610.1:n.290+59_290+60insA
NM_000455.4:c.290+59_290+60insA , LRG_319t1:c.290+59_290+60insA	NP_000446.1:n.290+59_290+60insA
XM_005259617.1:c.290+59_290+60insA	XP_005259674.1:n.290+59_290+60insA
XM_005259618.3:c.290+59_290+60insA	XP_005259675.1:n.290+59_290+60insA
XM_011528209.1:c.-64+59_-64+60insA	XP_011526511.1:n.-64+59_-64+60insA
XR_936204.1:n.915+59_915+60insA
XM_005259617.3:c.290+59_290+60insA	XP_005259674.1:n.290+59_290+60insA
XM_011528209.2:c.-64+59_-64+60insA	XP_011526511.1:n.-64+59_-64+60insA
XR_001753738.2:n.915+59_915+60insA
XR_001753739.1:n.915+59_915+60insA
XR_001753740.2:n.915+59_915+60insA
NM_000455.5:c.290+59_290+60insA MANE Select	NP_000446.1:n.290+59_290+60insA