Canonical Allele Identifier: CA2582597011
Gene: STK11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226217_1226218dup , CM000681.2:g.1226217_1226218dup GRCh38
NC_000019.9:g.1226216_1226217dup , CM000681.1:g.1226216_1226217dup GRCh37
NC_000019.8:g.1177216_1177217dup NCBI36
NG_007460.2:g.41811_41812dup , LRG_319:g.41811_41812dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.*2473_*2474dup ENSP00000490268.2:n.*2473_*2474dup
ENST00000585748.3:c.737-237_737-236dup ENSP00000477641.2:n.737-237_737-236dup
ENST00000585851.2:c.935-237_935-236dup ENSP00000467912.2:n.935-237_935-236dup
ENST00000326873.12:c.1109-237_1109-236dup MANE Select ENSP00000324856.6:n.1109-237_1109-236dup
ENST00000326873.11:c.1109-237_1109-236dup ENSP00000324856.6:n.1109-237_1109-236dup
ENST00000585465.2:n.2605_2606dup
ENST00000586243.5:c.1109-237_1109-236dup ENSP00000467240.2:n.1109-237_1109-236dup
ENST00000589152.5:n.1807-237_1807-236dup
NM_000455.4:c.1109-237_1109-236dup , LRG_319t1:c.1109-237_1109-236dup NP_000446.1:n.1109-237_1109-236dup
XM_005259617.1:c.1109-242_1109-241dup XP_005259674.1:n.1109-242_1109-241dup
XM_011528209.1:c.887-242_887-241dup XP_011526511.1:n.887-242_887-241dup
XM_005259617.3:c.1109-242_1109-241dup XP_005259674.1:n.1109-242_1109-241dup
XM_011528209.2:c.887-242_887-241dup XP_011526511.1:n.887-242_887-241dup
XR_001753738.2:n.1915-237_1915-236dup
XR_001753740.2:n.1885-237_1885-236dup
NM_000455.5:c.1109-237_1109-236dup MANE Select NP_000446.1:n.1109-237_1109-236dup