Canonical Allele Identifier: CA022211

Gene: STK11

Linked Data

• ClinVar Variation Id: 141851
• ClinVar RCV Id: RCV000130534 ; RCV000217158 ; RCV000527203
• dbSNP Id: rs587782058
• MyVariant Identifiers: chr19:g.1223103C>G (hg19) ; chr19:g.1223104C>G (hg38)
• PubMed: PMID:26976419

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223104C>G , CM000681.2:g.1223104C>G	GRCh38
NC_000019.9:g.1223103C>G , CM000681.1:g.1223103C>G	GRCh37
NC_000019.8:g.1174103C>G	NCBI36
NG_007460.2:g.38698C>G , LRG_319:g.38698C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1040C>G	ENSP00000490268.2:p.Ala347Gly
ENST00000585748.3:c.668C>G	ENSP00000477641.2:p.Ala223Gly
ENST00000585851.2:c.866C>G	ENSP00000467912.2:p.Ala289Gly
ENST00000326873.12:c.1040C>G MANE Select	ENSP00000324856.6:p.Ala347Gly
ENST00000652231.1:c.1040C>G	ENSP00000498804.1:p.Ala347Gly
ENST00000326873.11:c.1040C>G	ENSP00000324856.6:p.Ala347Gly
ENST00000586243.5:c.1040C>G	ENSP00000467240.2:p.Ala347Gly
ENST00000589152.5:n.1738C>G
ENST00000591133.2:n.1011C>G
NM_000455.4:c.1040C>G , LRG_319t1:c.1040C>G	NP_000446.1:p.Ala347Gly
XM_005259617.1:c.1040C>G	XP_005259674.1:p.Ala347Gly
XM_005259618.3:c.1040C>G	XP_005259675.1:p.Ala347Gly
XM_011528209.1:c.818C>G	XP_011526511.1:p.Ala273Gly
XR_936204.1:n.1816C>G
XM_005259617.3:c.1040C>G	XP_005259674.1:p.Ala347Gly
XM_011528209.2:c.818C>G	XP_011526511.1:p.Ala273Gly
XR_001753738.2:n.1846C>G
XR_001753739.1:n.1846C>G
XR_001753740.2:n.1816C>G
NM_000455.5:c.1040C>G MANE Select	NP_000446.1:p.Ala347Gly