Canonical Allele Identifier: CA2695227943
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1223088dup , CM000681.2:g.1223088dup GRCh38
NC_000019.9:g.1223087dup , CM000681.1:g.1223087dup GRCh37
NC_000019.8:g.1174087dup NCBI36
NG_007460.2:g.38682dup , LRG_319:g.38682dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.1024dup ENSP00000490268.2:p.Glu342GlyfsTer18
ENST00000585748.3:c.652dup ENSP00000477641.2:p.Glu218GlyfsTer18
ENST00000585851.2:c.850dup ENSP00000467912.2:p.Glu284GlyfsTer18
ENST00000326873.12:c.1024dup MANE Select ENSP00000324856.6:p.Glu342GlyfsTer18
ENST00000652231.1:c.1024dup ENSP00000498804.1:p.Glu342GlyfsTer18
ENST00000326873.11:c.1024dup ENSP00000324856.6:p.Glu342GlyfsTer18
ENST00000586243.5:c.1024dup ENSP00000467240.2:p.Glu342GlyfsTer18
ENST00000589152.5:n.1722dup
ENST00000591133.2:n.995dup
NM_000455.4:c.1024dup , LRG_319t1:c.1024dup NP_000446.1:p.Glu342GlyfsTer18
XM_005259617.1:c.1024dup XP_005259674.1:p.Glu342GlyfsTer18
XM_005259618.3:c.1024dup XP_005259675.1:p.Glu342GlyfsTer18
XM_011528209.1:c.802dup XP_011526511.1:p.Glu268GlyfsTer18
XR_936204.1:n.1800dup
XM_005259617.3:c.1024dup XP_005259674.1:p.Glu342GlyfsTer18
XM_011528209.2:c.802dup XP_011526511.1:p.Glu268GlyfsTer18
XR_001753738.2:n.1830dup
XR_001753739.1:n.1830dup
XR_001753740.2:n.1800dup
NM_000455.5:c.1024dup MANE Select NP_000446.1:p.Glu342GlyfsTer18