Canonical Allele Identifier: CA2735563111
Gene: STK11 HGNC NCBI

Linked Data

dbSNP Id: rs2145435526

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226381_1226382insT , CM000681.2:g.1226381_1226382insT GRCh38
NC_000019.9:g.1226380_1226381insT , CM000681.1:g.1226380_1226381insT GRCh37
NC_000019.8:g.1177380_1177381insT NCBI36
NG_007460.2:g.41975_41976insT , LRG_319:g.41975_41976insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.*2637_*2638insT ENSP00000490268.2:n.*2637_*2638insT
ENST00000585748.3:c.737-73_737-72insT ENSP00000477641.2:n.737-73_737-72insT
ENST00000585851.2:c.935-73_935-72insT ENSP00000467912.2:n.935-73_935-72insT
ENST00000326873.12:c.1109-73_1109-72insT MANE Select ENSP00000324856.6:n.1109-73_1109-72insT
ENST00000326873.11:c.1109-73_1109-72insT ENSP00000324856.6:n.1109-73_1109-72insT
ENST00000585465.2:n.2769_2770insT
ENST00000586243.5:c.1109-73_1109-72insT ENSP00000467240.2:n.1109-73_1109-72insT
ENST00000589152.5:n.1807-73_1807-72insT
NM_000455.4:c.1109-73_1109-72insT , LRG_319t1:c.1109-73_1109-72insT NP_000446.1:n.1109-73_1109-72insT
XM_005259617.1:c.1109-78_1109-77insT XP_005259674.1:n.1109-78_1109-77insT
XM_011528209.1:c.887-78_887-77insT XP_011526511.1:n.887-78_887-77insT
XM_005259617.3:c.1109-78_1109-77insT XP_005259674.1:n.1109-78_1109-77insT
XM_011528209.2:c.887-78_887-77insT XP_011526511.1:n.887-78_887-77insT
XR_001753738.2:n.1915-73_1915-72insT
XR_001753740.2:n.1885-73_1885-72insT
NM_000455.5:c.1109-73_1109-72insT MANE Select NP_000446.1:n.1109-73_1109-72insT