Canonical Allele Identifier: CA402954118

Gene: STK11

Linked Data

• ClinVar Variation Id: 1016338
• ClinVar RCV Id: RCV001315330
• dbSNP Id: rs751352435
• MyVariant Identifiers: chr19:g.1226610C>G (hg19) ; chr19:g.1226611C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226611C>G , CM000681.2:g.1226611C>G	GRCh38
NC_000019.9:g.1226610C>G , CM000681.1:g.1226610C>G	GRCh37
NC_000019.8:g.1177610C>G	NCBI36
NG_007460.2:g.42205C>G , LRG_319:g.42205C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2867C>G	ENSP00000490268.2:n.*2867C>G
ENST00000585748.3:c.894C>G	ENSP00000477641.2:p.Ser298Arg
ENST00000585851.2:c.1092C>G	ENSP00000467912.2:p.Ser364Arg
ENST00000326873.12:c.1266C>G MANE Select	ENSP00000324856.6:p.Ser422Arg
ENST00000326873.11:c.1266C>G	ENSP00000324856.6:p.Ser422Arg
ENST00000585465.2:n.2999C>G
ENST00000586243.5:c.1263C>G	ENSP00000467240.2:p.Ser421Arg
ENST00000589152.5:n.1964C>G
NM_000455.4:c.1266C>G , LRG_319t1:c.1266C>G	NP_000446.1:p.Ser422Arg
XM_005259617.1:c.1261C>G	XP_005259674.1:p.Gln421Glu
XM_011528209.1:c.1039C>G	XP_011526511.1:p.Gln347Glu
XM_005259617.3:c.1261C>G	XP_005259674.1:p.Gln421Glu
XM_011528209.2:c.1039C>G	XP_011526511.1:p.Gln347Glu
XR_001753738.2:n.2072C>G
XR_001753740.2:n.2042C>G
NM_000455.5:c.1266C>G MANE Select	NP_000446.1:p.Ser422Arg