Canonical Allele Identifier: CA2582591173
Gene: STK11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1206808_1206813del , CM000681.2:g.1206808_1206813del GRCh38
NC_000019.9:g.1206807_1206812del , CM000681.1:g.1206807_1206812del GRCh37
NC_000019.8:g.1157807_1157812del NCBI36
NG_007460.2:g.22402_22407del , LRG_319:g.22402_22407del

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.-106_-101del ENSP00000490268.2:n.-106_-101del
ENST00000585748.3:c.-82-11609_-82-11604del ENSP00000477641.2:n.-82-11609_-82-11604de...
ENST00000326873.12:c.-106_-101del MANE Select ENSP00000324856.6:n.-106_-101del
ENST00000652231.1:c.-106_-101del ENSP00000498804.1:n.-106_-101del
ENST00000326873.11:c.-106_-101del ENSP00000324856.6:n.-106_-101del
ENST00000585748.2:c.-82-11609_-82-11604del ENSP00000477641.1:n.-82-11609_-82-11604de...
ENST00000586243.5:c.-106_-101del ENSP00000467240.2:n.-106_-101del
NM_000455.4:c.-106_-101del , LRG_319t1:c.-106_-101del NP_000446.1:n.-106_-101del
XM_005259617.1:c.-106_-101del XP_005259674.1:n.-106_-101del
XM_005259618.3:c.-106_-101del XP_005259675.1:n.-106_-101del
XM_011528209.1:c.-459_-454del XP_011526511.1:n.-459_-454del
XR_936204.1:n.520_525del
XM_005259617.3:c.-106_-101del XP_005259674.1:n.-106_-101del
XM_011528209.2:c.-459_-454del XP_011526511.1:n.-459_-454del
XR_001753738.2:n.520_525del
XR_001753739.1:n.520_525del
XR_001753740.2:n.520_525del
NM_000455.5:c.-106_-101del MANE Select NP_000446.1:n.-106_-101del