Canonical Allele Identifier: CA891844255

Gene: STK11

Linked Data

• ClinVar Variation Id: 576260
• ClinVar RCV Id: RCV000698721 ; RCV002343505
• dbSNP Id: rs1568707668

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220449_1220451delinsGAA , CM000681.2:g.1220449_1220451delinsGAA	GRCh38
NC_000019.9:g.1220448_1220450delinsGAA , CM000681.1:g.1220448_1220450delinsGAA	GRCh37
NC_000019.8:g.1171448_1171450delinsGAA	NCBI36
NG_007460.2:g.36043_36045delinsGAA , LRG_319:g.36043_36045delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.541_543delinsGAA	ENSP00000490268.2:p.Asn181Glu
ENST00000585748.3:c.169_171delinsGAA	ENSP00000477641.2:p.Asn57Glu
ENST00000585851.2:c.367_369delinsGAA	ENSP00000467912.2:p.Asn123Glu
ENST00000326873.12:c.541_543delinsGAA MANE Select	ENSP00000324856.6:p.Asn181Glu
ENST00000652231.1:c.541_543delinsGAA	ENSP00000498804.1:p.Asn181Glu
ENST00000326873.11:c.541_543delinsGAA	ENSP00000324856.6:p.Asn181Glu
ENST00000585851.1:c.367_369delinsGAA	ENSP00000467912.1:p.Asn123Glu
ENST00000586243.5:c.541_543delinsGAA	ENSP00000467240.2:p.Asn181Glu
ENST00000586358.5:n.364_366delinsGAA
ENST00000589152.5:n.631_633delinsGAA
ENST00000591133.2:n.437_439delinsGAA
NM_000455.4:c.541_543delinsGAA , LRG_319t1:c.541_543delinsGAA	NP_000446.1:p.Asn181Glu
XM_005259617.1:c.541_543delinsGAA	XP_005259674.1:p.Asn181Glu
XM_005259618.3:c.541_543delinsGAA	XP_005259675.1:p.Asn181Glu
XM_011528209.1:c.319_321delinsGAA	XP_011526511.1:p.Asn107Glu
XR_936204.1:n.1166_1168delinsGAA
XM_005259617.3:c.541_543delinsGAA	XP_005259674.1:p.Asn181Glu
XM_011528209.2:c.319_321delinsGAA	XP_011526511.1:p.Asn107Glu
XR_001753738.2:n.1166_1168delinsGAA
XR_001753739.1:n.1166_1168delinsGAA
XR_001753740.2:n.1166_1168delinsGAA
NM_000455.5:c.541_543delinsGAA MANE Select	NP_000446.1:p.Asn181Glu