Canonical Allele Identifier: CA631299712
Gene: STK11 HGNC NCBI

Linked Data

dbSNP Id: rs1430123512

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1206812_1206818del , CM000681.2:g.1206812_1206818del GRCh38
NC_000019.9:g.1206811_1206817del , CM000681.1:g.1206811_1206817del GRCh37
NC_000019.8:g.1157811_1157817del NCBI36
NG_007460.2:g.22406_22412del , LRG_319:g.22406_22412del

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.-102_-96del ENSP00000490268.2:n.-102_-96del
ENST00000585748.3:c.-82-11605_-82-11599del ENSP00000477641.2:n.-82-11605_-82-11599de...
ENST00000326873.12:c.-102_-96del MANE Select ENSP00000324856.6:n.-102_-96del
ENST00000652231.1:c.-102_-96del ENSP00000498804.1:n.-102_-96del
ENST00000326873.11:c.-102_-96del ENSP00000324856.6:n.-102_-96del
ENST00000585748.2:c.-82-11605_-82-11599del ENSP00000477641.1:n.-82-11605_-82-11599de...
ENST00000586243.5:c.-102_-96del ENSP00000467240.2:n.-102_-96del
NM_000455.4:c.-102_-96del , LRG_319t1:c.-102_-96del NP_000446.1:n.-102_-96del
XM_005259617.1:c.-102_-96del XP_005259674.1:n.-102_-96del
XM_005259618.3:c.-102_-96del XP_005259675.1:n.-102_-96del
XM_011528209.1:c.-455_-449del XP_011526511.1:n.-455_-449del
XR_936204.1:n.524_530del
XM_005259617.3:c.-102_-96del XP_005259674.1:n.-102_-96del
XM_011528209.2:c.-455_-449del XP_011526511.1:n.-455_-449del
XR_001753738.2:n.524_530del
XR_001753739.1:n.524_530del
XR_001753740.2:n.524_530del
NM_000455.5:c.-102_-96del MANE Select NP_000446.1:n.-102_-96del