Canonical Allele Identifier: CA3047144217
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226594dup , CM000681.2:g.1226594dup GRCh38
NC_000019.9:g.1226593dup , CM000681.1:g.1226593dup GRCh37
NC_000019.8:g.1177593dup NCBI36
NG_007460.2:g.42188dup , LRG_319:g.42188dup

Transcript Alleles

HGVS Amino-acid Change
NM_000455.5:c.1249dup MANE Select NP_000446.1:p.Ala417GlyfsTer?
ENST00000326873.12:c.1249dup MANE Select ENSP00000324856.6:p.Ala417GlyfsTer?
NM_000455.4:c.1249dup , LRG_319t1:c.1249dup NP_000446.1:p.Ala417GlyfsTer?
ENST00000326873.11:c.1249dup ENSP00000324856.6:p.Ala417GlyfsTer?
ENST00000585465.2:n.2982dup
ENST00000585465.3:c.*2850dup ENSP00000490268.2:n.*2850dup
ENST00000585748.3:c.877dup ENSP00000477641.2:p.Ala293GlyfsTer?
ENST00000585851.2:c.1075dup ENSP00000467912.2:p.Ala359GlyfsTer?
ENST00000586243.5:c.1248dup ENSP00000467240.2:p.Pro417AlafsTer?
ENST00000589152.5:n.1947dup
XM_005259617.1:c.1244dup XP_005259674.1:p.Leu416ProfsTer?
XM_005259617.3:c.1244dup XP_005259674.1:p.Leu416ProfsTer?
XM_011528209.1:c.1022dup XP_011526511.1:p.Leu342ProfsTer?
XM_011528209.2:c.1022dup XP_011526511.1:p.Leu342ProfsTer?
XR_001753738.2:n.2055dup
XR_001753740.2:n.2025dup