Canonical Allele Identifier: CA402954018

Gene: STK11

Linked Data

• ClinVar Variation Id: 527827
• ClinVar RCV Id: RCV001182961 ; RCV000632824
• dbSNP Id: rs1166243253
• MyVariant Identifiers: chr19:g.1226594C>G (hg19) ; chr19:g.1226595C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226595C>G , CM000681.2:g.1226595C>G	GRCh38
NC_000019.9:g.1226594C>G , CM000681.1:g.1226594C>G	GRCh37
NC_000019.8:g.1177594C>G	NCBI36
NG_007460.2:g.42189C>G , LRG_319:g.42189C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2851C>G	ENSP00000490268.2:n.*2851C>G
ENST00000585748.3:c.878C>G	ENSP00000477641.2:p.Ala293Gly
ENST00000585851.2:c.1076C>G	ENSP00000467912.2:p.Ala359Gly
ENST00000326873.12:c.1250C>G MANE Select	ENSP00000324856.6:p.Ala417Gly
ENST00000326873.11:c.1250C>G	ENSP00000324856.6:p.Ala417Gly
ENST00000585465.2:n.2983C>G
ENST00000586243.5:c.1249C>G	ENSP00000467240.2:p.Pro417Ala
ENST00000589152.5:n.1948C>G
NM_000455.4:c.1250C>G , LRG_319t1:c.1250C>G	NP_000446.1:p.Ala417Gly
XM_005259617.1:c.1245C>G	XP_005259674.1:p.Gly415=
XM_011528209.1:c.1023C>G	XP_011526511.1:p.Gly341=
XM_005259617.3:c.1245C>G	XP_005259674.1:p.Gly415=
XM_011528209.2:c.1023C>G	XP_011526511.1:p.Gly341=
XR_001753738.2:n.2056C>G
XR_001753740.2:n.2026C>G
NM_000455.5:c.1250C>G MANE Select	NP_000446.1:p.Ala417Gly