Canonical Allele Identifier: CA2695227959
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1221270dup , CM000681.2:g.1221270dup GRCh38
NC_000019.9:g.1221269dup , CM000681.1:g.1221269dup GRCh37
NC_000019.8:g.1172269dup NCBI36
NG_007460.2:g.36864dup , LRG_319:g.36864dup

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.792dup ENSP00000490268.2:p.Glu265Ter
ENST00000585748.3:c.420dup ENSP00000477641.2:p.Glu141Ter
ENST00000585851.2:c.618dup ENSP00000467912.2:p.Glu207Ter
ENST00000326873.12:c.792dup MANE Select ENSP00000324856.6:p.Glu265Ter
ENST00000652231.1:c.792dup ENSP00000498804.1:p.Glu265Ter
ENST00000326873.11:c.792dup ENSP00000324856.6:p.Glu265Ter
ENST00000586243.5:c.792dup ENSP00000467240.2:p.Glu265Ter
ENST00000586358.5:n.690dup
ENST00000589152.5:n.882dup
ENST00000591133.2:n.763dup
NM_000455.4:c.792dup , LRG_319t1:c.792dup NP_000446.1:p.Glu265Ter
XM_005259617.1:c.792dup XP_005259674.1:p.Glu265Ter
XM_005259618.3:c.792dup XP_005259675.1:p.Glu265Ter
XM_011528209.1:c.570dup XP_011526511.1:p.Glu191Ter
XR_936204.1:n.1417dup
XM_005259617.3:c.792dup XP_005259674.1:p.Glu265Ter
XM_011528209.2:c.570dup XP_011526511.1:p.Glu191Ter
XR_001753738.2:n.1417dup
XR_001753739.1:n.1417dup
XR_001753740.2:n.1417dup
NM_000455.5:c.792dup MANE Select NP_000446.1:p.Glu265Ter