Canonical Allele Identifier: CA2317588514
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1218415A= , CM000681.2:g.1218415A= GRCh38
NC_000019.9:g.1218414A= , CM000681.1:g.1218414A= GRCh37
NC_000019.8:g.1169414A= NCBI36
NG_007460.2:g.34009A= , LRG_319:g.34009A=

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.291-2A= ENSP00000490268.2:n.291-2A=
ENST00000585748.3:c.-82-2A= ENSP00000477641.2:n.-82-2A=
ENST00000585851.2:c.291-1958A= ENSP00000467912.2:n.291-1958A=
ENST00000326873.12:c.291-2A= MANE Select ENSP00000324856.6:n.291-2A=
ENST00000652231.1:c.291-2A= ENSP00000498804.1:n.291-2A=
ENST00000326873.11:c.291-2A= ENSP00000324856.6:n.291-2A=
ENST00000585748.2:c.-82-2A= ENSP00000477641.1:n.-82-2A=
ENST00000585851.1:c.291-1958A= ENSP00000467912.1:n.291-1958A=
ENST00000586243.5:c.291-2A= ENSP00000467240.2:n.291-2A=
ENST00000586358.5:n.114-2A=
ENST00000589152.5:n.381-2A=
ENST00000593219.5:c.*116-2A= ENSP00000466610.1:n.*116-2A=
NM_000455.4:c.291-2A= , LRG_319t1:c.291-2A= NP_000446.1:n.291-2A=
XM_005259617.1:c.291-2A= XP_005259674.1:n.291-2A=
XM_005259618.3:c.291-2A= XP_005259675.1:n.291-2A=
XM_011528209.1:c.69-2A= XP_011526511.1:n.69-2A=
XR_936204.1:n.916-2A=
XM_005259617.3:c.291-2A= XP_005259674.1:n.291-2A=
XM_011528209.2:c.69-2A= XP_011526511.1:n.69-2A=
XR_001753738.2:n.916-2A=
XR_001753739.1:n.916-2A=
XR_001753740.2:n.916-2A=
NM_000455.5:c.291-2A= MANE Select NP_000446.1:n.291-2A=