Canonical Allele Identifier: CA402953392

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226498G>T , CM000681.2:g.1226498G>T	GRCh38
NC_000019.9:g.1226497G>T , CM000681.1:g.1226497G>T	GRCh37
NC_000019.8:g.1177497G>T	NCBI36
NG_007460.2:g.42092G>T , LRG_319:g.42092G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1153G>T MANE Select	NP_000446.1:p.Gly385Cys
ENST00000326873.12:c.1153G>T MANE Select	ENSP00000324856.6:p.Gly385Cys
NM_000455.4:c.1153G>T , LRG_319t1:c.1153G>T	NP_000446.1:p.Gly385Cys
ENST00000326873.11:c.1153G>T	ENSP00000324856.6:p.Gly385Cys
ENST00000585465.2:n.2886G>T
ENST00000585465.3:c.*2754G>T	ENSP00000490268.2:n.*2754G>T
ENST00000585748.3:c.781G>T	ENSP00000477641.2:p.Gly261Cys
ENST00000585851.2:c.979G>T	ENSP00000467912.2:p.Gly327Cys
ENST00000586243.5:c.1153G>T	ENSP00000467240.2:p.Gly385Cys
ENST00000589152.5:n.1851G>T
XM_005259617.1:c.1148G>T	XP_005259674.1:p.Gly383Val
XM_005259617.3:c.1148G>T	XP_005259674.1:p.Gly383Val
XM_011528209.1:c.926G>T	XP_011526511.1:p.Gly309Val
XM_011528209.2:c.926G>T	XP_011526511.1:p.Gly309Val
XR_001753738.2:n.1959G>T
XR_001753740.2:n.1929G>T