Canonical Allele Identifier: CA2499225358

Gene: STK11

Linked Data

• ClinVar Variation Id: 1138289
• ClinVar RCV Id: RCV001474572 ; RCV001525825
• dbSNP Id: rs1407794756
• gnomAD v4: 19-1226450-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226450C>A , CM000681.2:g.1226450C>A	GRCh38
NC_000019.9:g.1226449C>A , CM000681.1:g.1226449C>A	GRCh37
NC_000019.8:g.1177449C>A	NCBI36
NG_007460.2:g.42044C>A , LRG_319:g.42044C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2706C>A	ENSP00000490268.2:n.*2706C>A
ENST00000585748.3:c.737-4C>A	ENSP00000477641.2:n.737-4C>A
ENST00000585851.2:c.935-4C>A	ENSP00000467912.2:n.935-4C>A
ENST00000326873.12:c.1109-4C>A MANE Select	ENSP00000324856.6:n.1109-4C>A
ENST00000326873.11:c.1109-4C>A	ENSP00000324856.6:n.1109-4C>A
ENST00000585465.2:n.2838C>A
ENST00000586243.5:c.1109-4C>A	ENSP00000467240.2:n.1109-4C>A
ENST00000589152.5:n.1807-4C>A
NM_000455.4:c.1109-4C>A , LRG_319t1:c.1109-4C>A	NP_000446.1:n.1109-4C>A
XM_005259617.1:c.1109-9C>A	XP_005259674.1:n.1109-9C>A
XM_011528209.1:c.887-9C>A	XP_011526511.1:n.887-9C>A
XM_005259617.3:c.1109-9C>A	XP_005259674.1:n.1109-9C>A
XM_011528209.2:c.887-9C>A	XP_011526511.1:n.887-9C>A
XR_001753738.2:n.1915-4C>A
XR_001753740.2:n.1885-4C>A
NM_000455.5:c.1109-4C>A MANE Select	NP_000446.1:n.1109-4C>A