Canonical Allele Identifier: CA402953707

Gene: STK11

Linked Data

• ClinVar Variation Id: 3231732
• ClinVar RCV Id: RCV004518447
• dbSNP Id: rs750055790
• MyVariant Identifiers: chr19:g.1226549C>A (hg19) ; chr19:g.1226550C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2806C>A	ENSP00000490268.2:n.*2806C>A
ENST00000585748.3:c.833C>A	ENSP00000477641.2:p.Thr278Asn
ENST00000585851.2:c.1031C>A	ENSP00000467912.2:p.Thr344Asn
ENST00000326873.12:c.1205C>A MANE Select	ENSP00000324856.6:p.Thr402Asn
ENST00000326873.11:c.1205C>A	ENSP00000324856.6:p.Thr402Asn
ENST00000585465.2:n.2938C>A
ENST00000586243.5:c.1205C>A	ENSP00000467240.2:p.Thr402Asn
ENST00000589152.5:n.1903C>A
NM_000455.4:c.1205C>A , LRG_319t1:c.1205C>A	NP_000446.1:p.Thr402Asn
XM_005259617.1:c.1200C>A	XP_005259674.1:p.His400Gln
XM_011528209.1:c.978C>A	XP_011526511.1:p.His326Gln
XM_005259617.3:c.1200C>A	XP_005259674.1:p.His400Gln
XM_011528209.2:c.978C>A	XP_011526511.1:p.His326Gln
XR_001753738.2:n.2011C>A
XR_001753740.2:n.1981C>A
NM_000455.5:c.1205C>A MANE Select	NP_000446.1:p.Thr402Asn