Canonical Allele Identifier: CA402953703

Gene: STK11

Linked Data

• ClinVar Variation Id: 2121742
• ClinVar RCV Id: RCV003043349
• gnomAD v4: 19-1226549-A-G
• MyVariant Identifiers: chr19:g.1226548A>G (hg19) ; chr19:g.1226549A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226549A>G , CM000681.2:g.1226549A>G	GRCh38
NC_000019.9:g.1226548A>G , CM000681.1:g.1226548A>G	GRCh37
NC_000019.8:g.1177548A>G	NCBI36
NG_007460.2:g.42143A>G , LRG_319:g.42143A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.*2805A>G	ENSP00000490268.2:n.*2805A>G
ENST00000585748.3:c.832A>G	ENSP00000477641.2:p.Thr278Ala
ENST00000585851.2:c.1030A>G	ENSP00000467912.2:p.Thr344Ala
ENST00000326873.12:c.1204A>G MANE Select	ENSP00000324856.6:p.Thr402Ala
ENST00000326873.11:c.1204A>G	ENSP00000324856.6:p.Thr402Ala
ENST00000585465.2:n.2937A>G
ENST00000586243.5:c.1204A>G	ENSP00000467240.2:p.Thr402Ala
ENST00000589152.5:n.1902A>G
NM_000455.4:c.1204A>G , LRG_319t1:c.1204A>G	NP_000446.1:p.Thr402Ala
XM_005259617.1:c.1199A>G	XP_005259674.1:p.His400Arg
XM_011528209.1:c.977A>G	XP_011526511.1:p.His326Arg
XM_005259617.3:c.1199A>G	XP_005259674.1:p.His400Arg
XM_011528209.2:c.977A>G	XP_011526511.1:p.His326Arg
XR_001753738.2:n.2010A>G
XR_001753740.2:n.1980A>G
NM_000455.5:c.1204A>G MANE Select	NP_000446.1:p.Thr402Ala