Canonical Allele Identifier: CA046784

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207229_1207234del , CM000681.2:g.1207229_1207234del	GRCh38
NC_000019.9:g.1207228_1207233del , CM000681.1:g.1207228_1207233del	GRCh37
NC_000019.8:g.1158228_1158233del	NCBI36
NG_007460.2:g.22823_22828del , LRG_319:g.22823_22828del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.290+26_290+31del	ENSP00000490268.2:n.290+26_290+31del
ENST00000585748.3:c.-82-11188_-82-11183del	ENSP00000477641.2:n.-82-11188_-82-11183del
ENST00000585851.2:c.290+26_290+31del	ENSP00000467912.2:n.290+26_290+31del
ENST00000326873.12:c.290+26_290+31del MANE Select	ENSP00000324856.6:n.290+26_290+31del
ENST00000652231.1:c.290+26_290+31del	ENSP00000498804.1:n.290+26_290+31del
ENST00000326873.11:c.290+26_290+31del	ENSP00000324856.6:n.290+26_290+31del
ENST00000585748.2:c.-82-11188_-82-11183del	ENSP00000477641.1:n.-82-11188_-82-11183del
ENST00000585851.1:c.290+26_290+31del	ENSP00000467912.1:n.290+26_290+31del
ENST00000586243.5:c.290+26_290+31del	ENSP00000467240.2:n.290+26_290+31del
ENST00000586358.5:n.113+26_113+31del
ENST00000589152.5:n.380+26_380+31del
ENST00000593219.5:c.290+26_290+31del	ENSP00000466610.1:n.290+26_290+31del
NM_000455.4:c.290+26_290+31del , LRG_319t1:c.290+26_290+31del	NP_000446.1:n.290+26_290+31del
XM_005259617.1:c.290+26_290+31del	XP_005259674.1:n.290+26_290+31del
XM_005259618.3:c.290+26_290+31del	XP_005259675.1:n.290+26_290+31del
XM_011528209.1:c.-64+26_-64+31del	XP_011526511.1:n.-64+26_-64+31del
XR_936204.1:n.915+26_915+31del
XM_005259617.3:c.290+26_290+31del	XP_005259674.1:n.290+26_290+31del
XM_011528209.2:c.-64+26_-64+31del	XP_011526511.1:n.-64+26_-64+31del
XR_001753738.2:n.915+26_915+31del
XR_001753739.1:n.915+26_915+31del
XR_001753740.2:n.915+26_915+31del
NM_000455.5:c.290+26_290+31del MANE Select	NP_000446.1:n.290+26_290+31del