Canonical Allele Identifier: CA023250

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220704G>A , CM000681.2:g.1220704G>A	GRCh38
NC_000019.9:g.1220703G>A , CM000681.1:g.1220703G>A	GRCh37
NC_000019.8:g.1171703G>A	NCBI36
NG_007460.2:g.36298G>A , LRG_319:g.36298G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.721G>A MANE Select	NP_000446.1:p.Ala241Thr
ENST00000326873.12:c.721G>A MANE Select	ENSP00000324856.6:p.Ala241Thr
NM_000455.4:c.721G>A , LRG_319t1:c.721G>A	NP_000446.1:p.Ala241Thr
ENST00000326873.11:c.721G>A	ENSP00000324856.6:p.Ala241Thr
ENST00000585465.3:c.721G>A	ENSP00000490268.2:p.Ala241Thr
ENST00000585748.3:c.349G>A	ENSP00000477641.2:p.Ala117Thr
ENST00000585851.2:c.547G>A	ENSP00000467912.2:p.Ala183Thr
ENST00000586243.5:c.721G>A	ENSP00000467240.2:p.Ala241Thr
ENST00000586358.5:n.619G>A
ENST00000589152.5:n.811G>A
ENST00000591133.2:n.692G>A
ENST00000652231.1:c.721G>A	ENSP00000498804.1:p.Ala241Thr
XM_005259617.1:c.721G>A	XP_005259674.1:p.Ala241Thr
XM_005259617.3:c.721G>A	XP_005259674.1:p.Ala241Thr
XM_005259618.3:c.721G>A	XP_005259675.1:p.Ala241Thr
XM_011528209.1:c.499G>A	XP_011526511.1:p.Ala167Thr
XM_011528209.2:c.499G>A	XP_011526511.1:p.Ala167Thr
XR_001753738.2:n.1346G>A
XR_001753739.1:n.1346G>A
XR_001753740.2:n.1346G>A
XR_936204.1:n.1346G>A