Canonical Allele Identifier: CA2695227932
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1223023dup , CM000681.2:g.1223023dup GRCh38
NC_000019.9:g.1223022dup , CM000681.1:g.1223022dup GRCh37
NC_000019.8:g.1174022dup NCBI36
NG_007460.2:g.38617dup , LRG_319:g.38617dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.959dup ENSP00000490268.2:p.Pro321AlafsTer?
ENST00000585748.3:c.587dup ENSP00000477641.2:p.Pro197AlafsTer?
ENST00000585851.2:c.785dup ENSP00000467912.2:p.Pro263AlafsTer?
ENST00000326873.12:c.959dup MANE Select ENSP00000324856.6:p.Pro321AlafsTer?
ENST00000652231.1:c.959dup ENSP00000498804.1:p.Pro321AlafsTer?
ENST00000326873.11:c.959dup ENSP00000324856.6:p.Pro321AlafsTer?
ENST00000586243.5:c.959dup ENSP00000467240.2:p.Pro321AlafsTer?
ENST00000589152.5:n.1657dup
ENST00000591133.2:n.930dup
NM_000455.4:c.959dup , LRG_319t1:c.959dup NP_000446.1:p.Pro321AlafsTer?
XM_005259617.1:c.959dup XP_005259674.1:p.Pro321AlafsTer?
XM_005259618.3:c.959dup XP_005259675.1:p.Pro321AlafsTer?
XM_011528209.1:c.737dup XP_011526511.1:p.Pro247AlafsTer?
XR_936204.1:n.1735dup
XM_005259617.3:c.959dup XP_005259674.1:p.Pro321AlafsTer?
XM_011528209.2:c.737dup XP_011526511.1:p.Pro247AlafsTer?
XR_001753738.2:n.1765dup
XR_001753739.1:n.1765dup
XR_001753740.2:n.1735dup
NM_000455.5:c.959dup MANE Select NP_000446.1:p.Pro321AlafsTer?