Canonical Allele Identifier: CA2317593438
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226131_1226132delinsGC , CM000681.2:g.1226131_1226132delinsGC GRCh38
NC_000019.9:g.1226130_1226131delinsGC , CM000681.1:g.1226130_1226131delinsGC GRCh37
NC_000019.8:g.1177130_1177131delinsGC NCBI36
NG_007460.2:g.41725_41726delinsGC , LRG_319:g.41725_41726delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.*2387_*2388delinsGC ENSP00000490268.2:n.*2387_*2388delinsGC
ENST00000585748.3:c.737-323_737-322delinsGC ENSP00000477641.2:n.737-323_737-322delinsGC
ENST00000585851.2:c.935-323_935-322delinsGC ENSP00000467912.2:n.935-323_935-322delinsGC
ENST00000326873.12:c.1109-323_1109-322delinsGC MANE Select ENSP00000324856.6:n.1109-323_1109-322delinsGC
ENST00000326873.11:c.1109-323_1109-322delinsGC ENSP00000324856.6:n.1109-323_1109-322delinsGC
ENST00000585465.2:n.2519_2520delinsGC
ENST00000586243.5:c.1109-323_1109-322delinsGC ENSP00000467240.2:n.1109-323_1109-322delinsGC
ENST00000589152.5:n.1807-323_1807-322delinsGC
NM_000455.4:c.1109-323_1109-322delinsGC , LRG_319t1:c.1109-323_1109-322delinsGC NP_000446.1:n.1109-323_1109-322delinsGC
XM_005259617.1:c.1109-328_1109-327delinsGC XP_005259674.1:n.1109-328_1109-327delinsGC
XM_011528209.1:c.887-328_887-327delinsGC XP_011526511.1:n.887-328_887-327delinsGC
XM_005259617.3:c.1109-328_1109-327delinsGC XP_005259674.1:n.1109-328_1109-327delinsGC
XM_011528209.2:c.887-328_887-327delinsGC XP_011526511.1:n.887-328_887-327delinsGC
XR_001753738.2:n.1915-323_1915-322delinsGC
XR_001753740.2:n.1885-323_1885-322delinsGC
NM_000455.5:c.1109-323_1109-322delinsGC MANE Select NP_000446.1:n.1109-323_1109-322delinsGC