Canonical Allele Identifier: CA16620750

Gene: STK11

Linked Data

• ClinVar Variation Id: 421017
• ClinVar RCV Id: RCV000482087 ; RCV000807012 ; RCV002367637
• dbSNP Id: rs786201213
• COSMIC: COSM20869
• MyVariant Identifiers: chr19:g.1220612C>A (hg19) ; chr19:g.1220613C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220613C>A , CM000681.2:g.1220613C>A	GRCh38
NC_000019.9:g.1220612C>A , CM000681.1:g.1220612C>A	GRCh37
NC_000019.8:g.1171612C>A	NCBI36
NG_007460.2:g.36207C>A , LRG_319:g.36207C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.630C>A	ENSP00000490268.2:p.Cys210Ter
ENST00000585748.3:c.258C>A	ENSP00000477641.2:p.Cys86Ter
ENST00000585851.2:c.456C>A	ENSP00000467912.2:p.Cys152Ter
ENST00000326873.12:c.630C>A MANE Select	ENSP00000324856.6:p.Cys210Ter
ENST00000652231.1:c.630C>A	ENSP00000498804.1:p.Cys210Ter
ENST00000326873.11:c.630C>A	ENSP00000324856.6:p.Cys210Ter
ENST00000585851.1:c.456C>A	ENSP00000467912.1:p.Cys152Ter
ENST00000586243.5:c.630C>A	ENSP00000467240.2:p.Cys210Ter
ENST00000586358.5:n.528C>A
ENST00000589152.5:n.720C>A
ENST00000591133.2:n.601C>A
NM_000455.4:c.630C>A , LRG_319t1:c.630C>A	NP_000446.1:p.Cys210Ter
XM_005259617.1:c.630C>A	XP_005259674.1:p.Cys210Ter
XM_005259618.3:c.630C>A	XP_005259675.1:p.Cys210Ter
XM_011528209.1:c.408C>A	XP_011526511.1:p.Cys136Ter
XR_936204.1:n.1255C>A
XM_005259617.3:c.630C>A	XP_005259674.1:p.Cys210Ter
XM_011528209.2:c.408C>A	XP_011526511.1:p.Cys136Ter
XR_001753738.2:n.1255C>A
XR_001753739.1:n.1255C>A
XR_001753740.2:n.1255C>A
NM_000455.5:c.630C>A MANE Select	NP_000446.1:p.Cys210Ter