Canonical Allele Identifier: CA2697555602

Gene: STK11

Linked Data

• ClinVar Variation Id: 2763386
• ClinVar RCV Id: RCV003507754

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221226del , CM000681.2:g.1221226del	GRCh38
NC_000019.9:g.1221225del , CM000681.1:g.1221225del	GRCh37
NC_000019.8:g.1172225del	NCBI36
NG_007460.2:g.36820del , LRG_319:g.36820del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.748del	ENSP00000490268.2:p.Thr250ArgfsTer?
ENST00000585748.3:c.376del	ENSP00000477641.2:p.Thr126ArgfsTer?
ENST00000585851.2:c.574del	ENSP00000467912.2:p.Thr192ArgfsTer?
ENST00000326873.12:c.748del MANE Select	ENSP00000324856.6:p.Thr250ArgfsTer?
ENST00000652231.1:c.748del	ENSP00000498804.1:p.Thr250ArgfsTer?
ENST00000326873.11:c.748del	ENSP00000324856.6:p.Thr250ArgfsTer?
ENST00000586243.5:c.748del	ENSP00000467240.2:p.Thr250ArgfsTer?
ENST00000586358.5:n.646del
ENST00000589152.5:n.838del
ENST00000591133.2:n.719del
NM_000455.4:c.748del , LRG_319t1:c.748del	NP_000446.1:p.Thr250ArgfsTer?
XM_005259617.1:c.748del	XP_005259674.1:p.Thr250ArgfsTer?
XM_005259618.3:c.748del	XP_005259675.1:p.Thr250ArgfsTer?
XM_011528209.1:c.526del	XP_011526511.1:p.Thr176ArgfsTer?
XR_936204.1:n.1373del
XM_005259617.3:c.748del	XP_005259674.1:p.Thr250ArgfsTer?
XM_011528209.2:c.526del	XP_011526511.1:p.Thr176ArgfsTer?
XR_001753738.2:n.1373del
XR_001753739.1:n.1373del
XR_001753740.2:n.1373del
NM_000455.5:c.748del MANE Select	NP_000446.1:p.Thr250ArgfsTer?