Canonical Allele Identifier: CA2582591157
Gene: STK11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1206807_1206808insTTTTTTTTTTTT , CM000681.2:g.1206807_1206808insTTTTTTTTTTTT GRCh38
NC_000019.9:g.1206806_1206807insTTTTTTTTTTTT , CM000681.1:g.1206806_1206807insTTTTTTTTTTTT GRCh37
NC_000019.8:g.1157806_1157807insTTTTTTTTTTTT NCBI36
NG_007460.2:g.22401_22402insTTTTTTTTTTTT , LRG_319:g.22401_22402insTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.-107_-106insTTTTTTTTTTTT ENSP00000490268.2:n.-107_-106insTTTTTTTTTTTT
ENST00000585748.3:c.-82-11610_-82-11609insTTTTTTTTTTTT ENSP00000477641.2:n.-82-11610_-82-11609insTTTTTTTTTTTT
ENST00000326873.12:c.-107_-106insTTTTTTTTTTTT MANE Select ENSP00000324856.6:n.-107_-106insTTTTTTTTTTTT
ENST00000652231.1:c.-107_-106insTTTTTTTTTTTT ENSP00000498804.1:n.-107_-106insTTTTTTTTTTTT
ENST00000326873.11:c.-107_-106insTTTTTTTTTTTT ENSP00000324856.6:n.-107_-106insTTTTTTTTTTTT
ENST00000585748.2:c.-82-11610_-82-11609insTTTTTTTTTTTT ENSP00000477641.1:n.-82-11610_-82-11609insTTTTTTTTTTTT
ENST00000586243.5:c.-107_-106insTTTTTTTTTTTT ENSP00000467240.2:n.-107_-106insTTTTTTTTTTTT
NM_000455.4:c.-107_-106insTTTTTTTTTTTT , LRG_319t1:c.-107_-106insTTTTTTTTTTTT NP_000446.1:n.-107_-106insTTTTTTTTTTTT
XM_005259617.1:c.-107_-106insTTTTTTTTTTTT XP_005259674.1:n.-107_-106insTTTTTTTTTTTT
XM_005259618.3:c.-107_-106insTTTTTTTTTTTT XP_005259675.1:n.-107_-106insTTTTTTTTTTTT
XM_011528209.1:c.-460_-459insTTTTTTTTTTTT XP_011526511.1:n.-460_-459insTTTTTTTTTTTT
XR_936204.1:n.519_520insTTTTTTTTTTTT
XM_005259617.3:c.-107_-106insTTTTTTTTTTTT XP_005259674.1:n.-107_-106insTTTTTTTTTTTT
XM_011528209.2:c.-460_-459insTTTTTTTTTTTT XP_011526511.1:n.-460_-459insTTTTTTTTTTTT
XR_001753738.2:n.519_520insTTTTTTTTTTTT
XR_001753739.1:n.519_520insTTTTTTTTTTTT
XR_001753740.2:n.519_520insTTTTTTTTTTTT
NM_000455.5:c.-107_-106insTTTTTTTTTTTT MANE Select NP_000446.1:n.-107_-106insTTTTTTTTTTTT