Canonical Allele Identifier: CA1139666161

Gene: STK11

Linked Data

• ClinVar Variation Id: 965473
• ClinVar RCV Id: RCV001239930
• dbSNP Id: rs2080796043

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223018_1223020delinsCCAGGTGGGA , CM000681.2:g.1223018_1223020delinsCCAGGTGGGA	GRCh38
NC_000019.9:g.1223017_1223019delinsCCAGGTGGGA , CM000681.1:g.1223017_1223019delinsCCAGGTGGGA	GRCh37
NC_000019.8:g.1174017_1174019delinsCCAGGTGGGA	NCBI36
NG_007460.2:g.38612_38614delinsCCAGGTGGGA , LRG_319:g.38612_38614delinsCCAGGTGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.954_956delinsCCAGGTGGGA	ENSP00000490268.2:p.Pro319GlnfsTer?
ENST00000585748.3:c.582_584delinsCCAGGTGGGA	ENSP00000477641.2:p.Pro195GlnfsTer?
ENST00000585851.2:c.780_782delinsCCAGGTGGGA	ENSP00000467912.2:p.Pro261GlnfsTer?
ENST00000326873.12:c.954_956delinsCCAGGTGGGA MANE Select	ENSP00000324856.6:p.Pro319GlnfsTer?
ENST00000652231.1:c.954_956delinsCCAGGTGGGA	ENSP00000498804.1:p.Pro319GlnfsTer?
ENST00000326873.11:c.954_956delinsCCAGGTGGGA	ENSP00000324856.6:p.Pro319GlnfsTer?
ENST00000586243.5:c.954_956delinsCCAGGTGGGA	ENSP00000467240.2:p.Pro319GlnfsTer?
ENST00000589152.5:n.1652_1654delinsCCAGGTGGGA
ENST00000591133.2:n.925_927delinsCCAGGTGGGA
NM_000455.4:c.954_956delinsCCAGGTGGGA , LRG_319t1:c.954_956delinsCCAGGTGGGA	NP_000446.1:p.Pro319GlnfsTer?
XM_005259617.1:c.954_956delinsCCAGGTGGGA	XP_005259674.1:p.Pro319GlnfsTer?
XM_005259618.3:c.954_956delinsCCAGGTGGGA	XP_005259675.1:p.Pro319GlnfsTer?
XM_011528209.1:c.732_734delinsCCAGGTGGGA	XP_011526511.1:p.Pro245GlnfsTer?
XR_936204.1:n.1730_1732delinsCCAGGTGGGA
XM_005259617.3:c.954_956delinsCCAGGTGGGA	XP_005259674.1:p.Pro319GlnfsTer?
XM_011528209.2:c.732_734delinsCCAGGTGGGA	XP_011526511.1:p.Pro245GlnfsTer?
XR_001753738.2:n.1760_1762delinsCCAGGTGGGA
XR_001753739.1:n.1760_1762delinsCCAGGTGGGA
XR_001753740.2:n.1730_1732delinsCCAGGTGGGA
NM_000455.5:c.954_956delinsCCAGGTGGGA MANE Select	NP_000446.1:p.Pro319GlnfsTer?