Canonical Allele Identifier: CA402951345

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1222007G>C , CM000681.2:g.1222007G>C	GRCh38
NC_000019.9:g.1222006G>C , CM000681.1:g.1222006G>C	GRCh37
NC_000019.8:g.1173006G>C	NCBI36
NG_007460.2:g.37601G>C , LRG_319:g.37601G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.920+1G>C MANE Select	NP_000446.1:n.920+1G>C
ENST00000326873.12:c.920+1G>C MANE Select	ENSP00000324856.6:n.920+1G>C
NM_000455.4:c.920+1G>C , LRG_319t1:c.920+1G>C	NP_000446.1:n.920+1G>C
ENST00000326873.11:c.920+1G>C	ENSP00000324856.6:n.920+1G>C
ENST00000585465.3:c.920+1G>C	ENSP00000490268.2:n.920+1G>C
ENST00000585748.3:c.548+1G>C	ENSP00000477641.2:n.548+1G>C
ENST00000585851.2:c.746+1G>C	ENSP00000467912.2:n.746+1G>C
ENST00000586243.5:c.920+1G>C	ENSP00000467240.2:n.920+1G>C
ENST00000589152.5:n.1618+1G>C
ENST00000591133.2:n.891+1G>C
ENST00000652231.1:c.920+1G>C	ENSP00000498804.1:n.920+1G>C
XM_005259617.1:c.920+1G>C	XP_005259674.1:n.920+1G>C
XM_005259617.3:c.920+1G>C	XP_005259674.1:n.920+1G>C
XM_005259618.3:c.920+1G>C	XP_005259675.1:n.920+1G>C
XM_011528209.1:c.698+1G>C	XP_011526511.1:n.698+1G>C
XM_011528209.2:c.698+1G>C	XP_011526511.1:n.698+1G>C
XR_001753738.2:n.1726+1G>C
XR_001753739.1:n.1726+1G>C
XR_001753740.2:n.1696+1G>C
XR_936204.1:n.1696+1G>C