Canonical Allele Identifier: CA402953464

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226510G>A , CM000681.2:g.1226510G>A	GRCh38
NC_000019.9:g.1226509G>A , CM000681.1:g.1226509G>A	GRCh37
NC_000019.8:g.1177509G>A	NCBI36
NG_007460.2:g.42104G>A , LRG_319:g.42104G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1165G>A MANE Select	NP_000446.1:p.Ala389Thr
ENST00000326873.12:c.1165G>A MANE Select	ENSP00000324856.6:p.Ala389Thr
NM_000455.4:c.1165G>A , LRG_319t1:c.1165G>A	NP_000446.1:p.Ala389Thr
ENST00000326873.11:c.1165G>A	ENSP00000324856.6:p.Ala389Thr
ENST00000585465.2:n.2898G>A
ENST00000585465.3:c.*2766G>A	ENSP00000490268.2:n.*2766G>A
ENST00000585748.3:c.793G>A	ENSP00000477641.2:p.Ala265Thr
ENST00000585851.2:c.991G>A	ENSP00000467912.2:p.Ala331Thr
ENST00000586243.5:c.1165G>A	ENSP00000467240.2:p.Ala389Thr
ENST00000589152.5:n.1863G>A
XM_005259617.1:c.1160G>A	XP_005259674.1:p.Gly387Asp
XM_005259617.3:c.1160G>A	XP_005259674.1:p.Gly387Asp
XM_011528209.1:c.938G>A	XP_011526511.1:p.Gly313Asp
XM_011528209.2:c.938G>A	XP_011526511.1:p.Gly313Asp
XR_001753738.2:n.1971G>A
XR_001753740.2:n.1941G>A