Canonical Allele Identifier: CA2582591487

Gene: STK11

Linked Data

• gnomAD v4: 19-1207280-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207280_1207281insTT , CM000681.2:g.1207280_1207281insTT	GRCh38
NC_000019.9:g.1207279_1207280insTT , CM000681.1:g.1207279_1207280insTT	GRCh37
NC_000019.8:g.1158279_1158280insTT	NCBI36
NG_007460.2:g.22874_22875insTT , LRG_319:g.22874_22875insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.290+77_290+78insTT	ENSP00000490268.2:n.290+77_290+78insTT
ENST00000585748.3:c.-82-11137_-82-11136insTT	ENSP00000477641.2:n.-82-11137_-82-11136insTT
ENST00000585851.2:c.290+77_290+78insTT	ENSP00000467912.2:n.290+77_290+78insTT
ENST00000326873.12:c.290+77_290+78insTT MANE Select	ENSP00000324856.6:n.290+77_290+78insTT
ENST00000652231.1:c.290+77_290+78insTT	ENSP00000498804.1:n.290+77_290+78insTT
ENST00000326873.11:c.290+77_290+78insTT	ENSP00000324856.6:n.290+77_290+78insTT
ENST00000585748.2:c.-82-11137_-82-11136insTT	ENSP00000477641.1:n.-82-11137_-82-11136insTT
ENST00000585851.1:c.290+77_290+78insTT	ENSP00000467912.1:n.290+77_290+78insTT
ENST00000586243.5:c.290+77_290+78insTT	ENSP00000467240.2:n.290+77_290+78insTT
ENST00000586358.5:n.113+77_113+78insTT
ENST00000589152.5:n.380+77_380+78insTT
ENST00000593219.5:c.290+77_290+78insTT	ENSP00000466610.1:n.290+77_290+78insTT
NM_000455.4:c.290+77_290+78insTT , LRG_319t1:c.290+77_290+78insTT	NP_000446.1:n.290+77_290+78insTT
XM_005259617.1:c.290+77_290+78insTT	XP_005259674.1:n.290+77_290+78insTT
XM_005259618.3:c.290+77_290+78insTT	XP_005259675.1:n.290+77_290+78insTT
XM_011528209.1:c.-64+77_-64+78insTT	XP_011526511.1:n.-64+77_-64+78insTT
XR_936204.1:n.915+77_915+78insTT
XM_005259617.3:c.290+77_290+78insTT	XP_005259674.1:n.290+77_290+78insTT
XM_011528209.2:c.-64+77_-64+78insTT	XP_011526511.1:n.-64+77_-64+78insTT
XR_001753738.2:n.915+77_915+78insTT
XR_001753739.1:n.915+77_915+78insTT
XR_001753740.2:n.915+77_915+78insTT
NM_000455.5:c.290+77_290+78insTT MANE Select	NP_000446.1:n.290+77_290+78insTT