Canonical Allele Identifier: CA2317593764
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226594G= , CM000681.2:g.1226594G= GRCh38
NC_000019.9:g.1226593G= , CM000681.1:g.1226593G= GRCh37
NC_000019.8:g.1177593G= NCBI36
NG_007460.2:g.42188G= , LRG_319:g.42188G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.*2850G= ENSP00000490268.2:n.*2850G=
ENST00000585748.3:c.877G= ENSP00000477641.2:p.Ala293=
ENST00000585851.2:c.1075G= ENSP00000467912.2:p.Ala359=
ENST00000326873.12:c.1249G= MANE Select ENSP00000324856.6:p.Ala417=
ENST00000326873.11:c.1249G= ENSP00000324856.6:p.Ala417=
ENST00000585465.2:n.2982G=
ENST00000586243.5:c.1248G= ENSP00000467240.2:p.Arg416=
ENST00000589152.5:n.1947G=
NM_000455.4:c.1249G= , LRG_319t1:c.1249G= NP_000446.1:p.Ala417=
XM_005259617.1:c.1244G= XP_005259674.1:p.Gly415=
XM_011528209.1:c.1022G= XP_011526511.1:p.Gly341=
XM_005259617.3:c.1244G= XP_005259674.1:p.Gly415=
XM_011528209.2:c.1022G= XP_011526511.1:p.Gly341=
XR_001753738.2:n.2055G=
XR_001753740.2:n.2025G=
NM_000455.5:c.1249G= MANE Select NP_000446.1:p.Ala417=