Canonical Allele Identifier: CA2695227850
Gene: STK11 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.127dup ENSP00000490268.2:p.Ala43GlyfsTer?
ENST00000585748.3:c.-82-11377dup ENSP00000477641.2:n.-82-11377dup
ENST00000585851.2:c.127dup ENSP00000467912.2:p.Ala43GlyfsTer?
ENST00000326873.12:c.127dup MANE Select ENSP00000324856.6:p.Ala43GlyfsTer?
ENST00000652231.1:c.127dup ENSP00000498804.1:p.Ala43GlyfsTer?
ENST00000326873.11:c.127dup ENSP00000324856.6:p.Ala43GlyfsTer?
ENST00000585748.2:c.-82-11377dup ENSP00000477641.1:n.-82-11377dup
ENST00000585851.1:c.127dup ENSP00000467912.1:p.Ala43GlyfsTer?
ENST00000586243.5:c.127dup ENSP00000467240.2:p.Ala43GlyfsTer?
ENST00000589152.5:n.217dup
ENST00000593219.5:c.127dup ENSP00000466610.1:p.Ala43GlyfsTer?
NM_000455.4:c.127dup , LRG_319t1:c.127dup NP_000446.1:p.Ala43GlyfsTer?
XM_005259617.1:c.127dup XP_005259674.1:p.Ala43GlyfsTer?
XM_005259618.3:c.127dup XP_005259675.1:p.Ala43GlyfsTer?
XM_011528209.1:c.-227dup XP_011526511.1:n.-227dup
XR_936204.1:n.752dup
XM_005259617.3:c.127dup XP_005259674.1:p.Ala43GlyfsTer?
XM_011528209.2:c.-227dup XP_011526511.1:n.-227dup
XR_001753738.2:n.752dup
XR_001753739.1:n.752dup
XR_001753740.2:n.752dup
NM_000455.5:c.127dup MANE Select NP_000446.1:p.Ala43GlyfsTer?