Canonical Allele Identifier: CA2573155779

Gene: STK11

Linked Data

• ClinVar Variation Id: 1683509
• ClinVar RCV Id: RCV002243552
• dbSNP Id: rs2145430705

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223008del , CM000681.2:g.1223008del	GRCh38
NC_000019.9:g.1223007del , CM000681.1:g.1223007del	GRCh37
NC_000019.8:g.1174007del	NCBI36
NG_007460.2:g.38602del , LRG_319:g.38602del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.944del	ENSP00000490268.2:p.Pro315ArgfsTer21
ENST00000585748.3:c.572del	ENSP00000477641.2:p.Pro191ArgfsTer21
ENST00000585851.2:c.770del	ENSP00000467912.2:p.Pro257ArgfsTer21
ENST00000326873.12:c.944del MANE Select	ENSP00000324856.6:p.Pro315ArgfsTer21
ENST00000652231.1:c.944del	ENSP00000498804.1:p.Pro315ArgfsTer21
ENST00000326873.11:c.944del	ENSP00000324856.6:p.Pro315ArgfsTer21
ENST00000586243.5:c.944del	ENSP00000467240.2:p.Pro315ArgfsTer21
ENST00000589152.5:n.1642del
ENST00000591133.2:n.915del
NM_000455.4:c.944del , LRG_319t1:c.944del	NP_000446.1:p.Pro315ArgfsTer21
XM_005259617.1:c.944del	XP_005259674.1:p.Pro315ArgfsTer21
XM_005259618.3:c.944del	XP_005259675.1:p.Pro315ArgfsTer21
XM_011528209.1:c.722del	XP_011526511.1:p.Pro241ArgfsTer21
XR_936204.1:n.1720del
XM_005259617.3:c.944del	XP_005259674.1:p.Pro315ArgfsTer21
XM_011528209.2:c.722del	XP_011526511.1:p.Pro241ArgfsTer21
XR_001753738.2:n.1750del
XR_001753739.1:n.1750del
XR_001753740.2:n.1720del
NM_000455.5:c.944del MANE Select	NP_000446.1:p.Pro315ArgfsTer21