Canonical Allele Identifier: CA2582597429
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226499del , CM000681.2:g.1226499del GRCh38
NC_000019.9:g.1226498del , CM000681.1:g.1226498del GRCh37
NC_000019.8:g.1177498del NCBI36
NG_007460.2:g.42093del , LRG_319:g.42093del

Transcript Alleles

HGVS Amino-acid Change
NM_000455.5:c.1154del MANE Select NP_000446.1:p.Gly385AlafsTer8
ENST00000326873.12:c.1154del MANE Select ENSP00000324856.6:p.Gly385AlafsTer8
NM_000455.4:c.1154del , LRG_319t1:c.1154del NP_000446.1:p.Gly385AlafsTer8
ENST00000326873.11:c.1154del ENSP00000324856.6:p.Gly385AlafsTer8
ENST00000585465.2:n.2887del
ENST00000585465.3:c.*2755del ENSP00000490268.2:n.*2755del
ENST00000585748.3:c.782del ENSP00000477641.2:p.Gly261AlafsTer8
ENST00000585851.2:c.980del ENSP00000467912.2:p.Gly327AlafsTer8
ENST00000586243.5:c.1154del ENSP00000467240.2:p.Gly385AlafsTer8
ENST00000589152.5:n.1852del
XM_005259617.1:c.1149del XP_005259674.1:p.Pro384LeufsTer?
XM_005259617.3:c.1149del XP_005259674.1:p.Pro384LeufsTer?
XM_011528209.1:c.927del XP_011526511.1:p.Pro310LeufsTer?
XM_011528209.2:c.927del XP_011526511.1:p.Pro310LeufsTer?
XR_001753738.2:n.1960del
XR_001753740.2:n.1930del