Canonical Allele Identifier: CA045929

Gene: STK11

Linked Data

• ClinVar Variation Id: 403787
• ClinVar RCV Id: RCV000464100 ; RCV001420889 ; RCV002348256
• dbSNP Id: rs750055790
• ExAC: 19:1226549 C / G
• MyVariant Identifiers: chr19:g.1226549C>G (hg19) ; chr19:g.1226550C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226550C>G , CM000681.2:g.1226550C>G	GRCh38
NC_000019.9:g.1226549C>G , CM000681.1:g.1226549C>G	GRCh37
NC_000019.8:g.1177549C>G	NCBI36
NG_007460.2:g.42144C>G , LRG_319:g.42144C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2806C>G	ENSP00000490268.2:n.*2806C>G
ENST00000585748.3:c.833C>G	ENSP00000477641.2:p.Thr278Ser
ENST00000585851.2:c.1031C>G	ENSP00000467912.2:p.Thr344Ser
ENST00000326873.12:c.1205C>G MANE Select	ENSP00000324856.6:p.Thr402Ser
ENST00000326873.11:c.1205C>G	ENSP00000324856.6:p.Thr402Ser
ENST00000585465.2:n.2938C>G
ENST00000586243.5:c.1205C>G	ENSP00000467240.2:p.Thr402Ser
ENST00000589152.5:n.1903C>G
NM_000455.4:c.1205C>G , LRG_319t1:c.1205C>G	NP_000446.1:p.Thr402Ser
XM_005259617.1:c.1200C>G	XP_005259674.1:p.His400Gln
XM_011528209.1:c.978C>G	XP_011526511.1:p.His326Gln
XM_005259617.3:c.1200C>G	XP_005259674.1:p.His400Gln
XM_011528209.2:c.978C>G	XP_011526511.1:p.His326Gln
XR_001753738.2:n.2011C>G
XR_001753740.2:n.1981C>G
NM_000455.5:c.1205C>G MANE Select	NP_000446.1:p.Thr402Ser