Canonical Allele Identifier: CA16616035

Gene: STK11

Linked Data

• ClinVar Variation Id: 403762
• ClinVar RCV Id: RCV000464501
• dbSNP Id: rs1060499951
• MyVariant Identifiers: chr19:g.1226468A>G (hg19) ; chr19:g.1226469A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226469A>G , CM000681.2:g.1226469A>G	GRCh38
NC_000019.9:g.1226468A>G , CM000681.1:g.1226468A>G	GRCh37
NC_000019.8:g.1177468A>G	NCBI36
NG_007460.2:g.42063A>G , LRG_319:g.42063A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2725A>G	ENSP00000490268.2:n.*2725A>G
ENST00000585748.3:c.752A>G	ENSP00000477641.2:p.Glu251Gly
ENST00000585851.2:c.950A>G	ENSP00000467912.2:p.Glu317Gly
ENST00000326873.12:c.1124A>G MANE Select	ENSP00000324856.6:p.Glu375Gly
ENST00000326873.11:c.1124A>G	ENSP00000324856.6:p.Glu375Gly
ENST00000585465.2:n.2857A>G
ENST00000586243.5:c.1124A>G	ENSP00000467240.2:p.Glu375Gly
ENST00000589152.5:n.1822A>G
NM_000455.4:c.1124A>G , LRG_319t1:c.1124A>G	NP_000446.1:p.Glu375Gly
XM_005259617.1:c.1119A>G	XP_005259674.1:p.Arg373=
XM_011528209.1:c.897A>G	XP_011526511.1:p.Arg299=
XM_005259617.3:c.1119A>G	XP_005259674.1:p.Arg373=
XM_011528209.2:c.897A>G	XP_011526511.1:p.Arg299=
XR_001753738.2:n.1930A>G
XR_001753740.2:n.1900A>G
NM_000455.5:c.1124A>G MANE Select	NP_000446.1:p.Glu375Gly