Canonical Allele Identifier: CA022653

Gene: STK11

Linked Data

• ClinVar Variation Id: 182875
• ClinVar RCV Id: RCV000160967
• dbSNP Id: rs730881958
• MyVariant Identifiers: chr19:g.1207046_1207057del (hg19) ; chr19:g.1207047_1207058del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207047_1207058del , CM000681.2:g.1207047_1207058del	GRCh38
NC_000019.9:g.1207046_1207057del , CM000681.1:g.1207046_1207057del	GRCh37
NC_000019.8:g.1158046_1158057del	NCBI36
NG_007460.2:g.22641_22652del , LRG_319:g.22641_22652del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.134_145del	ENSP00000490268.2:p.Leu45_Tyr49delinsHis
ENST00000585748.3:c.-82-11370_-82-11359del	ENSP00000477641.2:n.-82-11370_-82-11359del
ENST00000585851.2:c.134_145del	ENSP00000467912.2:p.Leu45_Tyr49delinsHis
ENST00000326873.12:c.134_145del MANE Select	ENSP00000324856.6:p.Leu45_Tyr49delinsHis
ENST00000652231.1:c.134_145del	ENSP00000498804.1:p.Leu45_Tyr49delinsHis
ENST00000326873.11:c.134_145del	ENSP00000324856.6:p.Leu45_Tyr49delinsHis
ENST00000585748.2:c.-82-11370_-82-11359del	ENSP00000477641.1:n.-82-11370_-82-11359del
ENST00000585851.1:c.134_145del	ENSP00000467912.1:p.Leu45_Tyr49delinsHis
ENST00000586243.5:c.134_145del	ENSP00000467240.2:p.Leu45_Tyr49delinsHis
ENST00000589152.5:n.224_235del
ENST00000593219.5:c.134_145del	ENSP00000466610.1:p.Leu45_Tyr49delinsHis
NM_000455.4:c.134_145del , LRG_319t1:c.134_145del	NP_000446.1:p.Leu45_Tyr49delinsHis
XM_005259617.1:c.134_145del	XP_005259674.1:p.Leu45_Tyr49delinsHis
XM_005259618.3:c.134_145del	XP_005259675.1:p.Leu45_Tyr49delinsHis
XM_011528209.1:c.-220_-209del	XP_011526511.1:n.-220_-209del
XR_936204.1:n.759_770del
XM_005259617.3:c.134_145del	XP_005259674.1:p.Leu45_Tyr49delinsHis
XM_011528209.2:c.-220_-209del	XP_011526511.1:n.-220_-209del
XR_001753738.2:n.759_770del
XR_001753739.1:n.759_770del
XR_001753740.2:n.759_770del
NM_000455.5:c.134_145del MANE Select	NP_000446.1:p.Leu45_Tyr49delinsHis