Canonical Allele Identifier: CA2317588513
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1218414C= , CM000681.2:g.1218414C= GRCh38
NC_000019.9:g.1218413C= , CM000681.1:g.1218413C= GRCh37
NC_000019.8:g.1169413C= NCBI36
NG_007460.2:g.34008C= , LRG_319:g.34008C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.291-3C= ENSP00000490268.2:n.291-3C=
ENST00000585748.3:c.-82-3C= ENSP00000477641.2:n.-82-3C=
ENST00000585851.2:c.291-1959C= ENSP00000467912.2:n.291-1959C=
ENST00000326873.12:c.291-3C= MANE Select ENSP00000324856.6:n.291-3C=
ENST00000652231.1:c.291-3C= ENSP00000498804.1:n.291-3C=
ENST00000326873.11:c.291-3C= ENSP00000324856.6:n.291-3C=
ENST00000585748.2:c.-82-3C= ENSP00000477641.1:n.-82-3C=
ENST00000585851.1:c.291-1959C= ENSP00000467912.1:n.291-1959C=
ENST00000586243.5:c.291-3C= ENSP00000467240.2:n.291-3C=
ENST00000586358.5:n.114-3C=
ENST00000589152.5:n.381-3C=
ENST00000593219.5:c.*116-3C= ENSP00000466610.1:n.*116-3C=
NM_000455.4:c.291-3C= , LRG_319t1:c.291-3C= NP_000446.1:n.291-3C=
XM_005259617.1:c.291-3C= XP_005259674.1:n.291-3C=
XM_005259618.3:c.291-3C= XP_005259675.1:n.291-3C=
XM_011528209.1:c.69-3C= XP_011526511.1:n.69-3C=
XR_936204.1:n.916-3C=
XM_005259617.3:c.291-3C= XP_005259674.1:n.291-3C=
XM_011528209.2:c.69-3C= XP_011526511.1:n.69-3C=
XR_001753738.2:n.916-3C=
XR_001753739.1:n.916-3C=
XR_001753740.2:n.916-3C=
NM_000455.5:c.291-3C= MANE Select NP_000446.1:n.291-3C=