Canonical Allele Identifier: CA1139666178

Gene: STK11

Linked Data

• ClinVar Variation Id: 946279
• ClinVar RCV Id: RCV001217112
• dbSNP Id: rs2080670569

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206973_1206974delinsTT , CM000681.2:g.1206973_1206974delinsTT	GRCh38
NC_000019.9:g.1206972_1206973delinsTT , CM000681.1:g.1206972_1206973delinsTT	GRCh37
NC_000019.8:g.1157972_1157973delinsTT	NCBI36
NG_007460.2:g.22567_22568delinsTT , LRG_319:g.22567_22568delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.60_61delinsTT	ENSP00000490268.2:p.Gly21Cys
ENST00000585748.3:c.-82-11444_-82-11443delinsTT	ENSP00000477641.2:n.-82-11444_-82-11443delinsTT
ENST00000585851.2:c.60_61delinsTT	ENSP00000467912.2:p.Gly21Cys
ENST00000326873.12:c.60_61delinsTT MANE Select	ENSP00000324856.6:p.Gly21Cys
ENST00000652231.1:c.60_61delinsTT	ENSP00000498804.1:p.Gly21Cys
ENST00000326873.11:c.60_61delinsTT	ENSP00000324856.6:p.Gly21Cys
ENST00000585748.2:c.-82-11444_-82-11443delinsTT	ENSP00000477641.1:n.-82-11444_-82-11443delinsTT
ENST00000585851.1:c.60_61delinsTT	ENSP00000467912.1:p.Gly21Cys
ENST00000586243.5:c.60_61delinsTT	ENSP00000467240.2:p.Gly21Cys
ENST00000589152.5:n.150_151delinsTT
ENST00000593219.5:c.60_61delinsTT	ENSP00000466610.1:p.Gly21Cys
NM_000455.4:c.60_61delinsTT , LRG_319t1:c.60_61delinsTT	NP_000446.1:p.Gly21Cys
XM_005259617.1:c.60_61delinsTT	XP_005259674.1:p.Gly21Cys
XM_005259618.3:c.60_61delinsTT	XP_005259675.1:p.Gly21Cys
XM_011528209.1:c.-294_-293delinsTT	XP_011526511.1:n.-294_-293delinsTT
XR_936204.1:n.685_686delinsTT
XM_005259617.3:c.60_61delinsTT	XP_005259674.1:p.Gly21Cys
XM_011528209.2:c.-294_-293delinsTT	XP_011526511.1:n.-294_-293delinsTT
XR_001753738.2:n.685_686delinsTT
XR_001753739.1:n.685_686delinsTT
XR_001753740.2:n.685_686delinsTT
NM_000455.5:c.60_61delinsTT MANE Select	NP_000446.1:p.Gly21Cys