Canonical Allele Identifier: CA2580096143

Gene: STK11

Linked Data

• ClinVar Variation Id: 2032070
• ClinVar RCV Id: RCV002876712

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223106del , CM000681.2:g.1223106del	GRCh38
NC_000019.9:g.1223105del , CM000681.1:g.1223105del	GRCh37
NC_000019.8:g.1174105del	NCBI36
NG_007460.2:g.38700del , LRG_319:g.38700del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1042del	ENSP00000490268.2:p.Asp348ThrfsTer?
ENST00000585748.3:c.670del	ENSP00000477641.2:p.Asp224ThrfsTer?
ENST00000585851.2:c.868del	ENSP00000467912.2:p.Asp290ThrfsTer?
ENST00000326873.12:c.1042del MANE Select	ENSP00000324856.6:p.Asp348ThrfsTer?
ENST00000652231.1:c.1042del	ENSP00000498804.1:p.Asp348ThrfsTer?
ENST00000326873.11:c.1042del	ENSP00000324856.6:p.Asp348ThrfsTer?
ENST00000586243.5:c.1042del	ENSP00000467240.2:p.Asp348ThrfsTer?
ENST00000589152.5:n.1740del
NM_000455.4:c.1042del , LRG_319t1:c.1042del	NP_000446.1:p.Asp348ThrfsTer?
XM_005259617.1:c.1042del	XP_005259674.1:p.Asp348ThrfsTer?
XM_005259618.3:c.1042del	XP_005259675.1:p.Asp348ThrfsTer?
XM_011528209.1:c.820del	XP_011526511.1:p.Asp274ThrfsTer?
XR_936204.1:n.1818del
XM_005259617.3:c.1042del	XP_005259674.1:p.Asp348ThrfsTer?
XM_011528209.2:c.820del	XP_011526511.1:p.Asp274ThrfsTer?
XR_001753738.2:n.1848del
XR_001753739.1:n.1848del
XR_001753740.2:n.1818del
NM_000455.5:c.1042del MANE Select	NP_000446.1:p.Asp348ThrfsTer?