Canonical Allele Identifier: CA402953306

Gene: STK11

Linked Data

• ClinVar Variation Id: 458016
• ClinVar RCV Id: RCV000529286 ; RCV002456067
• dbSNP Id: rs1555740086
• gnomAD v4: 19-1226486-G-A
• MyVariant Identifiers: chr19:g.1226485G>A (hg19) ; chr19:g.1226486G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226486G>A , CM000681.2:g.1226486G>A	GRCh38
NC_000019.9:g.1226485G>A , CM000681.1:g.1226485G>A	GRCh37
NC_000019.8:g.1177485G>A	NCBI36
NG_007460.2:g.42080G>A , LRG_319:g.42080G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2742G>A	ENSP00000490268.2:n.*2742G>A
ENST00000585748.3:c.769G>A	ENSP00000477641.2:p.Gly257Arg
ENST00000585851.2:c.967G>A	ENSP00000467912.2:p.Gly323Arg
ENST00000326873.12:c.1141G>A MANE Select	ENSP00000324856.6:p.Gly381Arg
ENST00000326873.11:c.1141G>A	ENSP00000324856.6:p.Gly381Arg
ENST00000585465.2:n.2874G>A
ENST00000586243.5:c.1141G>A	ENSP00000467240.2:p.Gly381Arg
ENST00000589152.5:n.1839G>A
NM_000455.4:c.1141G>A , LRG_319t1:c.1141G>A	NP_000446.1:p.Gly381Arg
XM_005259617.1:c.1136G>A	XP_005259674.1:p.Trp379Ter
XM_011528209.1:c.914G>A	XP_011526511.1:p.Trp305Ter
XM_005259617.3:c.1136G>A	XP_005259674.1:p.Trp379Ter
XM_011528209.2:c.914G>A	XP_011526511.1:p.Trp305Ter
XR_001753738.2:n.1947G>A
XR_001753740.2:n.1917G>A
NM_000455.5:c.1141G>A MANE Select	NP_000446.1:p.Gly381Arg