Canonical Allele Identifier: CA047202
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1218494A>G , CM000681.2:g.1218494A>G GRCh38
NC_000019.9:g.1218493A>G , CM000681.1:g.1218493A>G GRCh37
NC_000019.8:g.1169493A>G NCBI36
NG_007460.2:g.34088A>G , LRG_319:g.34088A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.368A>G ENSP00000490268.2:p.Gln123Arg
ENST00000585748.3:c.-5A>G ENSP00000477641.2:n.-5A>G
ENST00000585851.2:c.291-1879A>G ENSP00000467912.2:n.291-1879A>G
ENST00000326873.12:c.368A>G MANE Select ENSP00000324856.6:p.Gln123Arg
ENST00000652231.1:c.368A>G ENSP00000498804.1:p.Gln123Arg
ENST00000326873.11:c.368A>G ENSP00000324856.6:p.Gln123Arg
ENST00000585748.2:c.-5A>G ENSP00000477641.1:n.-5A>G
ENST00000585851.1:c.291-1879A>G ENSP00000467912.1:n.291-1879A>G
ENST00000586243.5:c.368A>G ENSP00000467240.2:p.Gln123Arg
ENST00000586358.5:n.191A>G
ENST00000589152.5:n.458A>G
ENST00000593219.5:c.*193A>G ENSP00000466610.1:n.*193A>G
NM_000455.4:c.368A>G , LRG_319t1:c.368A>G NP_000446.1:p.Gln123Arg
XM_005259617.1:c.368A>G XP_005259674.1:p.Gln123Arg
XM_005259618.3:c.368A>G XP_005259675.1:p.Gln123Arg
XM_011528209.1:c.146A>G XP_011526511.1:p.Gln49Arg
XR_936204.1:n.993A>G
XM_005259617.3:c.368A>G XP_005259674.1:p.Gln123Arg
XM_011528209.2:c.146A>G XP_011526511.1:p.Gln49Arg
XR_001753738.2:n.993A>G
XR_001753739.1:n.993A>G
XR_001753740.2:n.993A>G
NM_000455.5:c.368A>G MANE Select NP_000446.1:p.Gln123Arg