Canonical Allele Identifier: CA2499225356

Gene: STK11

Linked Data

• ClinVar Variation Id: 1106130
• ClinVar RCV Id: RCV001430762
• dbSNP Id: rs922706582

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226447C>G , CM000681.2:g.1226447C>G	GRCh38
NC_000019.9:g.1226446C>G , CM000681.1:g.1226446C>G	GRCh37
NC_000019.8:g.1177446C>G	NCBI36
NG_007460.2:g.42041C>G , LRG_319:g.42041C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2703C>G	ENSP00000490268.2:n.*2703C>G
ENST00000585748.3:c.737-7C>G	ENSP00000477641.2:n.737-7C>G
ENST00000585851.2:c.935-7C>G	ENSP00000467912.2:n.935-7C>G
ENST00000326873.12:c.1109-7C>G MANE Select	ENSP00000324856.6:n.1109-7C>G
ENST00000326873.11:c.1109-7C>G	ENSP00000324856.6:n.1109-7C>G
ENST00000585465.2:n.2835C>G
ENST00000586243.5:c.1109-7C>G	ENSP00000467240.2:n.1109-7C>G
ENST00000589152.5:n.1807-7C>G
NM_000455.4:c.1109-7C>G , LRG_319t1:c.1109-7C>G	NP_000446.1:n.1109-7C>G
XM_005259617.1:c.1109-12C>G	XP_005259674.1:n.1109-12C>G
XM_011528209.1:c.887-12C>G	XP_011526511.1:n.887-12C>G
XM_005259617.3:c.1109-12C>G	XP_005259674.1:n.1109-12C>G
XM_011528209.2:c.887-12C>G	XP_011526511.1:n.887-12C>G
XR_001753738.2:n.1915-7C>G
XR_001753740.2:n.1885-7C>G
NM_000455.5:c.1109-7C>G MANE Select	NP_000446.1:n.1109-7C>G