Canonical Allele Identifier: CA2580096038

Gene: STK11

Linked Data

• ClinVar Variation Id: 2031134
• ClinVar RCV Id: RCV002872223

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207044_1207049del , CM000681.2:g.1207044_1207049del	GRCh38
NC_000019.9:g.1207043_1207048del , CM000681.1:g.1207043_1207048del	GRCh37
NC_000019.8:g.1158043_1158048del	NCBI36
NG_007460.2:g.22638_22643del , LRG_319:g.22638_22643del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.131_136del	ENSP00000490268.2:p.Lys44_Leu45del
ENST00000585748.3:c.-82-11373_-82-11368del	ENSP00000477641.2:n.-82-11373_-82-11368del
ENST00000585851.2:c.131_136del	ENSP00000467912.2:p.Lys44_Leu45del
ENST00000326873.12:c.131_136del MANE Select	ENSP00000324856.6:p.Lys44_Leu45del
ENST00000652231.1:c.131_136del	ENSP00000498804.1:p.Lys44_Leu45del
ENST00000326873.11:c.131_136del	ENSP00000324856.6:p.Lys44_Leu45del
ENST00000585748.2:c.-82-11373_-82-11368del	ENSP00000477641.1:n.-82-11373_-82-11368del
ENST00000585851.1:c.131_136del	ENSP00000467912.1:p.Lys44_Leu45del
ENST00000586243.5:c.131_136del	ENSP00000467240.2:p.Lys44_Leu45del
ENST00000589152.5:n.221_226del
ENST00000593219.5:c.131_136del	ENSP00000466610.1:p.Lys44_Leu45del
NM_000455.4:c.131_136del , LRG_319t1:c.131_136del	NP_000446.1:p.Lys44_Leu45del
XM_005259617.1:c.131_136del	XP_005259674.1:p.Lys44_Leu45del
XM_005259618.3:c.131_136del	XP_005259675.1:p.Lys44_Leu45del
XM_011528209.1:c.-223_-218del	XP_011526511.1:n.-223_-218del
XR_936204.1:n.756_761del
XM_005259617.3:c.131_136del	XP_005259674.1:p.Lys44_Leu45del
XM_011528209.2:c.-223_-218del	XP_011526511.1:n.-223_-218del
XR_001753738.2:n.756_761del
XR_001753739.1:n.756_761del
XR_001753740.2:n.756_761del
NM_000455.5:c.131_136del MANE Select	NP_000446.1:p.Lys44_Leu45del