Canonical Allele Identifier: CA402947859

Gene: STK11

Linked Data

• ClinVar Variation Id: 1009762
• ClinVar RCV Id: RCV001307294
• dbSNP Id: rs1205003744
• MyVariant Identifiers: chr19:g.1218484A>C (hg19) ; chr19:g.1218485A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218485A>C , CM000681.2:g.1218485A>C	GRCh38
NC_000019.9:g.1218484A>C , CM000681.1:g.1218484A>C	GRCh37
NC_000019.8:g.1169484A>C	NCBI36
NG_007460.2:g.34079A>C , LRG_319:g.34079A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.359A>C	ENSP00000490268.2:p.Glu120Ala
ENST00000585748.3:c.-14A>C	ENSP00000477641.2:n.-14A>C
ENST00000585851.2:c.291-1888A>C	ENSP00000467912.2:n.291-1888A>C
ENST00000326873.12:c.359A>C MANE Select	ENSP00000324856.6:p.Glu120Ala
ENST00000652231.1:c.359A>C	ENSP00000498804.1:p.Glu120Ala
ENST00000326873.11:c.359A>C	ENSP00000324856.6:p.Glu120Ala
ENST00000585748.2:c.-14A>C	ENSP00000477641.1:n.-14A>C
ENST00000585851.1:c.291-1888A>C	ENSP00000467912.1:n.291-1888A>C
ENST00000586243.5:c.359A>C	ENSP00000467240.2:p.Glu120Ala
ENST00000586358.5:n.182A>C
ENST00000589152.5:n.449A>C
ENST00000593219.5:c.*184A>C	ENSP00000466610.1:n.*184A>C
NM_000455.4:c.359A>C , LRG_319t1:c.359A>C	NP_000446.1:p.Glu120Ala
XM_005259617.1:c.359A>C	XP_005259674.1:p.Glu120Ala
XM_005259618.3:c.359A>C	XP_005259675.1:p.Glu120Ala
XM_011528209.1:c.137A>C	XP_011526511.1:p.Glu46Ala
XR_936204.1:n.984A>C
XM_005259617.3:c.359A>C	XP_005259674.1:p.Glu120Ala
XM_011528209.2:c.137A>C	XP_011526511.1:p.Glu46Ala
XR_001753738.2:n.984A>C
XR_001753739.1:n.984A>C
XR_001753740.2:n.984A>C
NM_000455.5:c.359A>C MANE Select	NP_000446.1:p.Glu120Ala