Canonical Allele Identifier: CA2317589841
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1220536G= , CM000681.2:g.1220536G= GRCh38
NC_000019.9:g.1220535G= , CM000681.1:g.1220535G= GRCh37
NC_000019.8:g.1171535G= NCBI36
NG_007460.2:g.36130G= , LRG_319:g.36130G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.597+31G= ENSP00000490268.2:n.597+31G=
ENST00000585748.3:c.225+31G= ENSP00000477641.2:n.225+31G=
ENST00000585851.2:c.423+31G= ENSP00000467912.2:n.423+31G=
ENST00000326873.12:c.597+31G= MANE Select ENSP00000324856.6:n.597+31G=
ENST00000652231.1:c.597+31G= ENSP00000498804.1:n.597+31G=
ENST00000326873.11:c.597+31G= ENSP00000324856.6:n.597+31G=
ENST00000585851.1:c.423+31G= ENSP00000467912.1:n.423+31G=
ENST00000586243.5:c.597+31G= ENSP00000467240.2:n.597+31G=
ENST00000586358.5:n.451G=
ENST00000589152.5:n.687+31G=
ENST00000591133.2:n.524G=
NM_000455.4:c.597+31G= , LRG_319t1:c.597+31G= NP_000446.1:n.597+31G=
XM_005259617.1:c.597+31G= XP_005259674.1:n.597+31G=
XM_005259618.3:c.597+31G= XP_005259675.1:n.597+31G=
XM_011528209.1:c.375+31G= XP_011526511.1:n.375+31G=
XR_936204.1:n.1222+31G=
XM_005259617.3:c.597+31G= XP_005259674.1:n.597+31G=
XM_011528209.2:c.375+31G= XP_011526511.1:n.375+31G=
XR_001753738.2:n.1222+31G=
XR_001753739.1:n.1222+31G=
XR_001753740.2:n.1222+31G=
NM_000455.5:c.597+31G= MANE Select NP_000446.1:n.597+31G=