Canonical Allele Identifier: CA402951843

Gene: STK11

Linked Data

• ClinVar Variation Id: 818292
• ClinVar RCV Id: RCV001009759
• dbSNP Id: rs1599929512
• MyVariant Identifiers: chr19:g.1223121T>G (hg19) ; chr19:g.1223122T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223122T>G , CM000681.2:g.1223122T>G	GRCh38
NC_000019.9:g.1223121T>G , CM000681.1:g.1223121T>G	GRCh37
NC_000019.8:g.1174121T>G	NCBI36
NG_007460.2:g.38716T>G , LRG_319:g.38716T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1058T>G	ENSP00000490268.2:p.Leu353Arg
ENST00000585748.3:c.686T>G	ENSP00000477641.2:p.Leu229Arg
ENST00000585851.2:c.884T>G	ENSP00000467912.2:p.Leu295Arg
ENST00000326873.12:c.1058T>G MANE Select	ENSP00000324856.6:p.Leu353Arg
ENST00000652231.1:c.1058T>G	ENSP00000498804.1:p.Leu353Arg
ENST00000326873.11:c.1058T>G	ENSP00000324856.6:p.Leu353Arg
ENST00000586243.5:c.1058T>G	ENSP00000467240.2:p.Leu353Arg
ENST00000589152.5:n.1756T>G
NM_000455.4:c.1058T>G , LRG_319t1:c.1058T>G	NP_000446.1:p.Leu353Arg
XM_005259617.1:c.1058T>G	XP_005259674.1:p.Leu353Arg
XM_005259618.3:c.1058T>G	XP_005259675.1:p.Leu353Arg
XM_011528209.1:c.836T>G	XP_011526511.1:p.Leu279Arg
XR_936204.1:n.1834T>G
XM_005259617.3:c.1058T>G	XP_005259674.1:p.Leu353Arg
XM_011528209.2:c.836T>G	XP_011526511.1:p.Leu279Arg
XR_001753738.2:n.1864T>G
XR_001753739.1:n.1864T>G
XR_001753740.2:n.1834T>G
NM_000455.5:c.1058T>G MANE Select	NP_000446.1:p.Leu353Arg