Canonical Allele Identifier: CA2739276343

Gene: STK11

Linked Data

• ClinVar Variation Id: 2849515
• ClinVar RCV Id: RCV003617424

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226435C>A , CM000681.2:g.1226435C>A	GRCh38
NC_000019.9:g.1226434C>A , CM000681.1:g.1226434C>A	GRCh37
NC_000019.8:g.1177434C>A	NCBI36
NG_007460.2:g.42029C>A , LRG_319:g.42029C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2691C>A	ENSP00000490268.2:n.*2691C>A
ENST00000585748.3:c.737-19C>A	ENSP00000477641.2:n.737-19C>A
ENST00000585851.2:c.935-19C>A	ENSP00000467912.2:n.935-19C>A
ENST00000326873.12:c.1109-19C>A MANE Select	ENSP00000324856.6:n.1109-19C>A
ENST00000326873.11:c.1109-19C>A	ENSP00000324856.6:n.1109-19C>A
ENST00000585465.2:n.2823C>A
ENST00000586243.5:c.1109-19C>A	ENSP00000467240.2:n.1109-19C>A
ENST00000589152.5:n.1807-19C>A
NM_000455.4:c.1109-19C>A , LRG_319t1:c.1109-19C>A	NP_000446.1:n.1109-19C>A
XM_005259617.1:c.1109-24C>A	XP_005259674.1:n.1109-24C>A
XM_011528209.1:c.887-24C>A	XP_011526511.1:n.887-24C>A
XM_005259617.3:c.1109-24C>A	XP_005259674.1:n.1109-24C>A
XM_011528209.2:c.887-24C>A	XP_011526511.1:n.887-24C>A
XR_001753738.2:n.1915-19C>A
XR_001753740.2:n.1885-19C>A
NM_000455.5:c.1109-19C>A MANE Select	NP_000446.1:n.1109-19C>A