Canonical Allele Identifier: CA402953341

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226489C>G , CM000681.2:g.1226489C>G	GRCh38
NC_000019.9:g.1226488C>G , CM000681.1:g.1226488C>G	GRCh37
NC_000019.8:g.1177488C>G	NCBI36
NG_007460.2:g.42083C>G , LRG_319:g.42083C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1144C>G MANE Select	NP_000446.1:p.Gln382Glu
ENST00000326873.12:c.1144C>G MANE Select	ENSP00000324856.6:p.Gln382Glu
NM_000455.4:c.1144C>G , LRG_319t1:c.1144C>G	NP_000446.1:p.Gln382Glu
ENST00000326873.11:c.1144C>G	ENSP00000324856.6:p.Gln382Glu
ENST00000585465.2:n.2877C>G
ENST00000585465.3:c.*2745C>G	ENSP00000490268.2:n.*2745C>G
ENST00000585748.3:c.772C>G	ENSP00000477641.2:p.Gln258Glu
ENST00000585851.2:c.970C>G	ENSP00000467912.2:p.Gln324Glu
ENST00000586243.5:c.1144C>G	ENSP00000467240.2:p.Gln382Glu
ENST00000589152.5:n.1842C>G
XM_005259617.1:c.1139C>G	XP_005259674.1:p.Thr380Arg
XM_005259617.3:c.1139C>G	XP_005259674.1:p.Thr380Arg
XM_011528209.1:c.917C>G	XP_011526511.1:p.Thr306Arg
XM_011528209.2:c.917C>G	XP_011526511.1:p.Thr306Arg
XR_001753738.2:n.1950C>G
XR_001753740.2:n.1920C>G