Canonical Allele Identifier: CA402951448
Gene: STK11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1222995A>G , CM000681.2:g.1222995A>G GRCh38
NC_000019.9:g.1222994A>G , CM000681.1:g.1222994A>G GRCh37
NC_000019.8:g.1173994A>G NCBI36
NG_007460.2:g.38589A>G , LRG_319:g.38589A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.931A>G ENSP00000490268.2:p.Lys311Glu
ENST00000585748.3:c.559A>G ENSP00000477641.2:p.Lys187Glu
ENST00000585851.2:c.757A>G ENSP00000467912.2:p.Lys253Glu
ENST00000326873.12:c.931A>G MANE Select ENSP00000324856.6:p.Lys311Glu
ENST00000652231.1:c.931A>G ENSP00000498804.1:p.Lys311Glu
ENST00000326873.11:c.931A>G ENSP00000324856.6:p.Lys311Glu
ENST00000586243.5:c.931A>G ENSP00000467240.2:p.Lys311Glu
ENST00000589152.5:n.1629A>G
ENST00000591133.2:n.902A>G
NM_000455.4:c.931A>G , LRG_319t1:c.931A>G NP_000446.1:p.Lys311Glu
XM_005259617.1:c.931A>G XP_005259674.1:p.Lys311Glu
XM_005259618.3:c.931A>G XP_005259675.1:p.Lys311Glu
XM_011528209.1:c.709A>G XP_011526511.1:p.Lys237Glu
XR_936204.1:n.1707A>G
XM_005259617.3:c.931A>G XP_005259674.1:p.Lys311Glu
XM_011528209.2:c.709A>G XP_011526511.1:p.Lys237Glu
XR_001753738.2:n.1737A>G
XR_001753739.1:n.1737A>G
XR_001753740.2:n.1707A>G
NM_000455.5:c.931A>G MANE Select NP_000446.1:p.Lys311Glu