Canonical Allele Identifier: CA2580096089

Gene: STK11

Linked Data

• ClinVar Variation Id: 1755385
• ClinVar RCV Id: RCV002369353

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220660del , CM000681.2:g.1220660del	GRCh38
NC_000019.9:g.1220659del , CM000681.1:g.1220659del	GRCh37
NC_000019.8:g.1171659del	NCBI36
NG_007460.2:g.36254del , LRG_319:g.36254del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.677del	ENSP00000490268.2:p.Asn226ThrfsTer?
ENST00000585748.3:c.305del	ENSP00000477641.2:p.Asn102ThrfsTer?
ENST00000585851.2:c.503del	ENSP00000467912.2:p.Asn168ThrfsTer?
ENST00000326873.12:c.677del MANE Select	ENSP00000324856.6:p.Asn226ThrfsTer?
ENST00000652231.1:c.677del	ENSP00000498804.1:p.Asn226ThrfsTer?
ENST00000326873.11:c.677del	ENSP00000324856.6:p.Asn226ThrfsTer?
ENST00000586243.5:c.677del	ENSP00000467240.2:p.Asn226ThrfsTer?
ENST00000586358.5:n.575del
ENST00000589152.5:n.767del
ENST00000591133.2:n.648del
NM_000455.4:c.677del , LRG_319t1:c.677del	NP_000446.1:p.Asn226ThrfsTer?
XM_005259617.1:c.677del	XP_005259674.1:p.Asn226ThrfsTer?
XM_005259618.3:c.677del	XP_005259675.1:p.Asn226ThrfsTer?
XM_011528209.1:c.455del	XP_011526511.1:p.Asn152ThrfsTer?
XR_936204.1:n.1302del
XM_005259617.3:c.677del	XP_005259674.1:p.Asn226ThrfsTer?
XM_011528209.2:c.455del	XP_011526511.1:p.Asn152ThrfsTer?
XR_001753738.2:n.1302del
XR_001753739.1:n.1302del
XR_001753740.2:n.1302del
NM_000455.5:c.677del MANE Select	NP_000446.1:p.Asn226ThrfsTer?