Canonical Allele Identifier: CA2695227866

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207200_1207210del , CM000681.2:g.1207200_1207210del	GRCh38
NC_000019.9:g.1207199_1207209del , CM000681.1:g.1207199_1207209del	GRCh37
NC_000019.8:g.1158199_1158209del	NCBI36
NG_007460.2:g.22794_22804del , LRG_319:g.22794_22804del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.287_290+7del
ENST00000585748.3:c.-82-11217_-82-11207del	ENSP00000477641.2:n.-82-11217_-82-11207del
ENST00000585851.2:c.287_290+7del
ENST00000326873.12:c.287_290+7del
ENST00000652231.1:c.287_290+7del
ENST00000326873.11:c.287_290+7del
ENST00000585748.2:c.-82-11217_-82-11207del	ENSP00000477641.1:n.-82-11217_-82-11207del
ENST00000585851.1:c.287_290+7del
ENST00000586243.5:c.287_290+7del
ENST00000586358.5:n.110_113+7del
ENST00000589152.5:n.377_380+7del
ENST00000593219.5:c.287_290+7del
NM_000455.4:c.287_290+7del , LRG_319t1:c.287_290+7del
XM_005259617.1:c.287_290+7del
XM_005259618.3:c.287_290+7del
XM_011528209.1:c.-67_-64+7del
XR_936204.1:n.912_915+7del
XM_005259617.3:c.287_290+7del
XM_011528209.2:c.-67_-64+7del
XR_001753738.2:n.912_915+7del
XR_001753739.1:n.912_915+7del
XR_001753740.2:n.912_915+7del
NM_000455.5:c.287_290+7del