Canonical Allele Identifier: CA2695227857

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207079_1207102del , CM000681.2:g.1207079_1207102del	GRCh38
NC_000019.9:g.1207078_1207101del , CM000681.1:g.1207078_1207101del	GRCh37
NC_000019.8:g.1158078_1158101del	NCBI36
NG_007460.2:g.22673_22696del , LRG_319:g.22673_22696del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.166_189del	ENSP00000490268.2:p.Gly56_Val63del
ENST00000585748.3:c.-82-11338_-82-11315del	ENSP00000477641.2:n.-82-11338_-82-11315del
ENST00000585851.2:c.166_189del	ENSP00000467912.2:p.Gly56_Val63del
ENST00000326873.12:c.166_189del MANE Select	ENSP00000324856.6:p.Gly56_Val63del
ENST00000652231.1:c.166_189del	ENSP00000498804.1:p.Gly56_Val63del
ENST00000326873.11:c.166_189del	ENSP00000324856.6:p.Gly56_Val63del
ENST00000585748.2:c.-82-11338_-82-11315del	ENSP00000477641.1:n.-82-11338_-82-11315del
ENST00000585851.1:c.166_189del	ENSP00000467912.1:p.Gly56_Val63del
ENST00000586243.5:c.166_189del	ENSP00000467240.2:p.Gly56_Val63del
ENST00000589152.5:n.256_279del
ENST00000593219.5:c.166_189del	ENSP00000466610.1:p.Gly56_Val63del
NM_000455.4:c.166_189del , LRG_319t1:c.166_189del	NP_000446.1:p.Gly56_Val63del
XM_005259617.1:c.166_189del	XP_005259674.1:p.Gly56_Val63del
XM_005259618.3:c.166_189del	XP_005259675.1:p.Gly56_Val63del
XM_011528209.1:c.-188_-165del	XP_011526511.1:n.-188_-165del
XR_936204.1:n.791_814del
XM_005259617.3:c.166_189del	XP_005259674.1:p.Gly56_Val63del
XM_011528209.2:c.-188_-165del	XP_011526511.1:n.-188_-165del
XR_001753738.2:n.791_814del
XR_001753739.1:n.791_814del
XR_001753740.2:n.791_814del
NM_000455.5:c.166_189del MANE Select	NP_000446.1:p.Gly56_Val63del