Canonical Allele Identifier: CA2317593709
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226531G= , CM000681.2:g.1226531G= GRCh38
NC_000019.9:g.1226530G= , CM000681.1:g.1226530G= GRCh37
NC_000019.8:g.1177530G= NCBI36
NG_007460.2:g.42125G= , LRG_319:g.42125G=

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.*2787G= ENSP00000490268.2:n.*2787G=
ENST00000585748.3:c.814G= ENSP00000477641.2:p.Glu272=
ENST00000585851.2:c.1012G= ENSP00000467912.2:p.Glu338=
ENST00000326873.12:c.1186G= MANE Select ENSP00000324856.6:p.Glu396=
ENST00000326873.11:c.1186G= ENSP00000324856.6:p.Glu396=
ENST00000585465.2:n.2919G=
ENST00000586243.5:c.1186G= ENSP00000467240.2:p.Glu396=
ENST00000589152.5:n.1884G=
NM_000455.4:c.1186G= , LRG_319t1:c.1186G= NP_000446.1:p.Glu396=
XM_005259617.1:c.1181G= XP_005259674.1:p.Arg394=
XM_011528209.1:c.959G= XP_011526511.1:p.Arg320=
XM_005259617.3:c.1181G= XP_005259674.1:p.Arg394=
XM_011528209.2:c.959G= XP_011526511.1:p.Arg320=
XR_001753738.2:n.1992G=
XR_001753740.2:n.1962G=
NM_000455.5:c.1186G= MANE Select NP_000446.1:p.Glu396=