Canonical Allele Identifier: CA2317593493
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226218_1226221delinsCGTG , CM000681.2:g.1226218_1226221delinsCGTG GRCh38
NC_000019.9:g.1226217_1226220delinsCGTG , CM000681.1:g.1226217_1226220delinsCGTG GRCh37
NC_000019.8:g.1177217_1177220delinsCGTG NCBI36
NG_007460.2:g.41812_41815delinsCGTG , LRG_319:g.41812_41815delinsCGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.*2474_*2477delinsCGTG ENSP00000490268.2:n.*2474_*2477delinsCGTG
ENST00000585748.3:c.737-236_737-233delinsCGTG ENSP00000477641.2:n.737-236_737-233delinsCGTG
ENST00000585851.2:c.935-236_935-233delinsCGTG ENSP00000467912.2:n.935-236_935-233delinsCGTG
ENST00000326873.12:c.1109-236_1109-233delinsCGTG MANE Select ENSP00000324856.6:n.1109-236_1109-233delinsCGTG
ENST00000326873.11:c.1109-236_1109-233delinsCGTG ENSP00000324856.6:n.1109-236_1109-233delinsCGTG
ENST00000585465.2:n.2606_2609delinsCGTG
ENST00000586243.5:c.1109-236_1109-233delinsCGTG ENSP00000467240.2:n.1109-236_1109-233delinsCGTG
ENST00000589152.5:n.1807-236_1807-233delinsCGTG
NM_000455.4:c.1109-236_1109-233delinsCGTG , LRG_319t1:c.1109-236_1109-233delinsCGTG NP_000446.1:n.1109-236_1109-233delinsCGTG
XM_005259617.1:c.1109-241_1109-238delinsCGTG XP_005259674.1:n.1109-241_1109-238delinsCGTG
XM_011528209.1:c.887-241_887-238delinsCGTG XP_011526511.1:n.887-241_887-238delinsCGTG
XM_005259617.3:c.1109-241_1109-238delinsCGTG XP_005259674.1:n.1109-241_1109-238delinsCGTG
XM_011528209.2:c.887-241_887-238delinsCGTG XP_011526511.1:n.887-241_887-238delinsCGTG
XR_001753738.2:n.1915-236_1915-233delinsCGTG
XR_001753740.2:n.1885-236_1885-233delinsCGTG
NM_000455.5:c.1109-236_1109-233delinsCGTG MANE Select NP_000446.1:n.1109-236_1109-233delinsCGTG