Canonical Allele Identifier: CA402951238

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221976G>A , CM000681.2:g.1221976G>A	GRCh38
NC_000019.9:g.1221975G>A , CM000681.1:g.1221975G>A	GRCh37
NC_000019.8:g.1172975G>A	NCBI36
NG_007460.2:g.37570G>A , LRG_319:g.37570G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.890G>A MANE Select	NP_000446.1:p.Arg297Lys
ENST00000326873.12:c.890G>A MANE Select	ENSP00000324856.6:p.Arg297Lys
NM_000455.4:c.890G>A , LRG_319t1:c.890G>A	NP_000446.1:p.Arg297Lys
ENST00000326873.11:c.890G>A	ENSP00000324856.6:p.Arg297Lys
ENST00000585465.3:c.890G>A	ENSP00000490268.2:p.Arg297Lys
ENST00000585748.3:c.518G>A	ENSP00000477641.2:p.Arg173Lys
ENST00000585851.2:c.716G>A	ENSP00000467912.2:p.Arg239Lys
ENST00000586243.5:c.890G>A	ENSP00000467240.2:p.Arg297Lys
ENST00000589152.5:n.1588G>A
ENST00000591133.2:n.861G>A
ENST00000652231.1:c.890G>A	ENSP00000498804.1:p.Arg297Lys
XM_005259617.1:c.890G>A	XP_005259674.1:p.Arg297Lys
XM_005259617.3:c.890G>A	XP_005259674.1:p.Arg297Lys
XM_005259618.3:c.890G>A	XP_005259675.1:p.Arg297Lys
XM_011528209.1:c.668G>A	XP_011526511.1:p.Arg223Lys
XM_011528209.2:c.668G>A	XP_011526511.1:p.Arg223Lys
XR_001753738.2:n.1696G>A
XR_001753739.1:n.1696G>A
XR_001753740.2:n.1666G>A
XR_936204.1:n.1666G>A