Canonical Allele Identifier: CA992502917
Gene: STK11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1206819_1206824del , CM000681.2:g.1206819_1206824del GRCh38
NC_000019.9:g.1206818_1206823del , CM000681.1:g.1206818_1206823del GRCh37
NC_000019.8:g.1157818_1157823del NCBI36
NG_007460.2:g.22413_22418del , LRG_319:g.22413_22418del

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.-95_-90del ENSP00000490268.2:n.-95_-90del
ENST00000585748.3:c.-82-11598_-82-11593del ENSP00000477641.2:n.-82-11598_-82-11593de...
ENST00000326873.12:c.-95_-90del MANE Select ENSP00000324856.6:n.-95_-90del
ENST00000652231.1:c.-95_-90del ENSP00000498804.1:n.-95_-90del
ENST00000326873.11:c.-95_-90del ENSP00000324856.6:n.-95_-90del
ENST00000585748.2:c.-82-11598_-82-11593del ENSP00000477641.1:n.-82-11598_-82-11593de...
ENST00000586243.5:c.-95_-90del ENSP00000467240.2:n.-95_-90del
ENST00000593219.5:c.-95_-90del ENSP00000466610.1:n.-95_-90del
NM_000455.4:c.-95_-90del , LRG_319t1:c.-95_-90del NP_000446.1:n.-95_-90del
XM_005259617.1:c.-95_-90del XP_005259674.1:n.-95_-90del
XM_005259618.3:c.-95_-90del XP_005259675.1:n.-95_-90del
XM_011528209.1:c.-448_-443del XP_011526511.1:n.-448_-443del
XR_936204.1:n.531_536del
XM_005259617.3:c.-95_-90del XP_005259674.1:n.-95_-90del
XM_011528209.2:c.-448_-443del XP_011526511.1:n.-448_-443del
XR_001753738.2:n.531_536del
XR_001753739.1:n.531_536del
XR_001753740.2:n.531_536del
NM_000455.5:c.-95_-90del MANE Select NP_000446.1:n.-95_-90del