Canonical Allele Identifier: CA402950446

Gene: STK11

Linked Data

• ClinVar Variation Id: 860411
• ClinVar RCV Id: RCV001066703
• dbSNP Id: rs2080781876
• MyVariant Identifiers: chr19:g.1221251C>A (hg19) ; chr19:g.1221252C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221252C>A , CM000681.2:g.1221252C>A	GRCh38
NC_000019.9:g.1221251C>A , CM000681.1:g.1221251C>A	GRCh37
NC_000019.8:g.1172251C>A	NCBI36
NG_007460.2:g.36846C>A , LRG_319:g.36846C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.774C>A	ENSP00000490268.2:p.Asp258Glu
ENST00000585748.3:c.402C>A	ENSP00000477641.2:p.Asp134Glu
ENST00000585851.2:c.600C>A	ENSP00000467912.2:p.Asp200Glu
ENST00000326873.12:c.774C>A MANE Select	ENSP00000324856.6:p.Asp258Glu
ENST00000652231.1:c.774C>A	ENSP00000498804.1:p.Asp258Glu
ENST00000326873.11:c.774C>A	ENSP00000324856.6:p.Asp258Glu
ENST00000586243.5:c.774C>A	ENSP00000467240.2:p.Asp258Glu
ENST00000586358.5:n.672C>A
ENST00000589152.5:n.864C>A
ENST00000591133.2:n.745C>A
NM_000455.4:c.774C>A , LRG_319t1:c.774C>A	NP_000446.1:p.Asp258Glu
XM_005259617.1:c.774C>A	XP_005259674.1:p.Asp258Glu
XM_005259618.3:c.774C>A	XP_005259675.1:p.Asp258Glu
XM_011528209.1:c.552C>A	XP_011526511.1:p.Asp184Glu
XR_936204.1:n.1399C>A
XM_005259617.3:c.774C>A	XP_005259674.1:p.Asp258Glu
XM_011528209.2:c.552C>A	XP_011526511.1:p.Asp184Glu
XR_001753738.2:n.1399C>A
XR_001753739.1:n.1399C>A
XR_001753740.2:n.1399C>A
NM_000455.5:c.774C>A MANE Select	NP_000446.1:p.Asp258Glu