Canonical Allele Identifier: CA2317581631
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1207040_1207041delinsGC , CM000681.2:g.1207040_1207041delinsGC GRCh38
NC_000019.9:g.1207039_1207040delinsGC , CM000681.1:g.1207039_1207040delinsGC GRCh37
NC_000019.8:g.1158039_1158040delinsGC NCBI36
NG_007460.2:g.22634_22635delinsGC , LRG_319:g.22634_22635delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.127_128delinsGC ENSP00000490268.2:p.Ala43=
ENST00000585748.3:c.-82-11377_-82-11376delinsGC ENSP00000477641.2:n.-82-11377_-82-11376delinsGC
ENST00000585851.2:c.127_128delinsGC ENSP00000467912.2:p.Ala43=
ENST00000326873.12:c.127_128delinsGC MANE Select ENSP00000324856.6:p.Ala43=
ENST00000652231.1:c.127_128delinsGC ENSP00000498804.1:p.Ala43=
ENST00000326873.11:c.127_128delinsGC ENSP00000324856.6:p.Ala43=
ENST00000585748.2:c.-82-11377_-82-11376delinsGC ENSP00000477641.1:n.-82-11377_-82-11376delinsGC
ENST00000585851.1:c.127_128delinsGC ENSP00000467912.1:p.Ala43=
ENST00000586243.5:c.127_128delinsGC ENSP00000467240.2:p.Ala43=
ENST00000589152.5:n.217_218delinsGC
ENST00000593219.5:c.127_128delinsGC ENSP00000466610.1:p.Ala43=
NM_000455.4:c.127_128delinsGC , LRG_319t1:c.127_128delinsGC NP_000446.1:p.Ala43=
XM_005259617.1:c.127_128delinsGC XP_005259674.1:p.Ala43=
XM_005259618.3:c.127_128delinsGC XP_005259675.1:p.Ala43=
XM_011528209.1:c.-227_-226delinsGC XP_011526511.1:n.-227_-226delinsGC
XR_936204.1:n.752_753delinsGC
XM_005259617.3:c.127_128delinsGC XP_005259674.1:p.Ala43=
XM_011528209.2:c.-227_-226delinsGC XP_011526511.1:n.-227_-226delinsGC
XR_001753738.2:n.752_753delinsGC
XR_001753739.1:n.752_753delinsGC
XR_001753740.2:n.752_753delinsGC
NM_000455.5:c.127_128delinsGC MANE Select NP_000446.1:p.Ala43=