Canonical Allele Identifier: CA2582591544

Gene: STK11

Linked Data

• gnomAD v4: 19-1207328-T-TGGCACGGAGGACACA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207331_1207332insACGGAGGACACAGGC , CM000681.2:g.1207331_1207332insACGGAGGACACAGGC	GRCh38
NC_000019.9:g.1207330_1207331insACGGAGGACACAGGC , CM000681.1:g.1207330_1207331insACGGAGGACACAGGC	GRCh37
NC_000019.8:g.1158330_1158331insACGGAGGACACAGGC	NCBI36
NG_007460.2:g.22925_22926insACGGAGGACACAGGC , LRG_319:g.22925_22926insACGGAGGACACAGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.290+128_290+129insACGGAGGACACAGGC	ENSP00000490268.2:n.290+128_290+129insACGGAGGACACAGGC
ENST00000585748.3:c.-82-11086_-82-11085insACGGAGGACACAGGC	ENSP00000477641.2:n.-82-11086_-82-11085insACGGAGGACACAGGC
ENST00000585851.2:c.290+128_290+129insACGGAGGACACAGGC	ENSP00000467912.2:n.290+128_290+129insACGGAGGACACAGGC
ENST00000326873.12:c.290+128_290+129insACGGAGGACACAGGC MANE Select	ENSP00000324856.6:n.290+128_290+129insACGGAGGACACAGGC
ENST00000652231.1:c.290+128_290+129insACGGAGGACACAGGC	ENSP00000498804.1:n.290+128_290+129insACGGAGGACACAGGC
ENST00000326873.11:c.290+128_290+129insACGGAGGACACAGGC	ENSP00000324856.6:n.290+128_290+129insACGGAGGACACAGGC
ENST00000585748.2:c.-82-11086_-82-11085insACGGAGGACACAGGC	ENSP00000477641.1:n.-82-11086_-82-11085insACGGAGGACACAGGC
ENST00000585851.1:c.290+128_290+129insACGGAGGACACAGGC	ENSP00000467912.1:n.290+128_290+129insACGGAGGACACAGGC
ENST00000586243.5:c.290+128_290+129insACGGAGGACACAGGC	ENSP00000467240.2:n.290+128_290+129insACGGAGGACACAGGC
ENST00000586358.5:n.113+128_113+129insACGGAGGACACAGGC
ENST00000589152.5:n.380+128_380+129insACGGAGGACACAGGC
ENST00000593219.5:c.290+128_290+129insACGGAGGACACAGGC	ENSP00000466610.1:n.290+128_290+129insACGGAGGACACAGGC
NM_000455.4:c.290+128_290+129insACGGAGGACACAGGC , LRG_319t1:c.290+128_290+129insACGGAGGACACAGGC	NP_000446.1:n.290+128_290+129insACGGAGGACACAGGC
XM_005259617.1:c.290+128_290+129insACGGAGGACACAGGC	XP_005259674.1:n.290+128_290+129insACGGAGGACACAGGC
XM_005259618.3:c.290+128_290+129insACGGAGGACACAGGC	XP_005259675.1:n.290+128_290+129insACGGAGGACACAGGC
XM_011528209.1:c.-64+128_-64+129insACGGAGGACACAGGC	XP_011526511.1:n.-64+128_-64+129insACGGAGGACACAGGC
XR_936204.1:n.915+128_915+129insACGGAGGACACAGGC
XM_005259617.3:c.290+128_290+129insACGGAGGACACAGGC	XP_005259674.1:n.290+128_290+129insACGGAGGACACAGGC
XM_011528209.2:c.-64+128_-64+129insACGGAGGACACAGGC	XP_011526511.1:n.-64+128_-64+129insACGGAGGACACAGGC
XR_001753738.2:n.915+128_915+129insACGGAGGACACAGGC
XR_001753739.1:n.915+128_915+129insACGGAGGACACAGGC
XR_001753740.2:n.915+128_915+129insACGGAGGACACAGGC
NM_000455.5:c.290+128_290+129insACGGAGGACACAGGC MANE Select	NP_000446.1:n.290+128_290+129insACGGAGGACACAGGC