Canonical Allele Identifier: CA402947884

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218489G>C , CM000681.2:g.1218489G>C	GRCh38
NC_000019.9:g.1218488G>C , CM000681.1:g.1218488G>C	GRCh37
NC_000019.8:g.1169488G>C	NCBI36
NG_007460.2:g.34083G>C , LRG_319:g.34083G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.363G>C MANE Select	NP_000446.1:p.Glu121Asp
ENST00000326873.12:c.363G>C MANE Select	ENSP00000324856.6:p.Glu121Asp
NM_000455.4:c.363G>C , LRG_319t1:c.363G>C	NP_000446.1:p.Glu121Asp
ENST00000326873.11:c.363G>C	ENSP00000324856.6:p.Glu121Asp
ENST00000585465.3:c.363G>C	ENSP00000490268.2:p.Glu121Asp
ENST00000585748.2:c.-10G>C	ENSP00000477641.1:n.-10G>C
ENST00000585748.3:c.-10G>C	ENSP00000477641.2:n.-10G>C
ENST00000585851.1:c.291-1884G>C	ENSP00000467912.1:n.291-1884G>C
ENST00000585851.2:c.291-1884G>C	ENSP00000467912.2:n.291-1884G>C
ENST00000586243.5:c.363G>C	ENSP00000467240.2:p.Glu121Asp
ENST00000586358.5:n.186G>C
ENST00000589152.5:n.453G>C
ENST00000593219.5:c.*188G>C	ENSP00000466610.1:n.*188G>C
ENST00000652231.1:c.363G>C	ENSP00000498804.1:p.Glu121Asp
XM_005259617.1:c.363G>C	XP_005259674.1:p.Glu121Asp
XM_005259617.3:c.363G>C	XP_005259674.1:p.Glu121Asp
XM_005259618.3:c.363G>C	XP_005259675.1:p.Glu121Asp
XM_011528209.1:c.141G>C	XP_011526511.1:p.Glu47Asp
XM_011528209.2:c.141G>C	XP_011526511.1:p.Glu47Asp
XR_001753738.2:n.988G>C
XR_001753739.1:n.988G>C
XR_001753740.2:n.988G>C
XR_936204.1:n.988G>C