Canonical Allele Identifier: CA2582592132
Gene: STK11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1219447_1219448insTGGCCGG , CM000681.2:g.1219447_1219448insTGGCCGG GRCh38
NC_000019.9:g.1219446_1219447insTGGCCGG , CM000681.1:g.1219446_1219447insTGGCCGG GRCh37
NC_000019.8:g.1170446_1170447insTGGCCGG NCBI36
NG_007460.2:g.35041_35042insTGGCCGG , LRG_319:g.35041_35042insTGGCCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.464+34_464+35insTGGCCGG ENSP00000490268.2:n.464+34_464+35insTGGCCGG
ENST00000585748.3:c.92+34_92+35insTGGCCGG ENSP00000477641.2:n.92+34_92+35insTGGCCGG
ENST00000585851.2:c.291-926_291-925insTGGCCGG ENSP00000467912.2:n.291-926_291-925insTGGCCGG
ENST00000326873.12:c.464+34_464+35insTGGCCGG MANE Select ENSP00000324856.6:n.464+34_464+35insTGGCCGG
ENST00000652231.1:c.464+34_464+35insTGGCCGG ENSP00000498804.1:n.464+34_464+35insTGGCCGG
ENST00000326873.11:c.464+34_464+35insTGGCCGG ENSP00000324856.6:n.464+34_464+35insTGGCCGG
ENST00000585851.1:c.291-926_291-925insTGGCCGG ENSP00000467912.1:n.291-926_291-925insTGGCCGG
ENST00000586243.5:c.464+34_464+35insTGGCCGG ENSP00000467240.2:n.464+34_464+35insTGGCCGG
ENST00000586358.5:n.287+34_287+35insTGGCCGG
ENST00000589152.5:n.554+34_554+35insTGGCCGG
NM_000455.4:c.464+34_464+35insTGGCCGG , LRG_319t1:c.464+34_464+35insTGGCCGG NP_000446.1:n.464+34_464+35insTGGCCGG
XM_005259617.1:c.464+34_464+35insTGGCCGG XP_005259674.1:n.464+34_464+35insTGGCCGG
XM_005259618.3:c.464+34_464+35insTGGCCGG XP_005259675.1:n.464+34_464+35insTGGCCGG
XM_011528209.1:c.242+34_242+35insTGGCCGG XP_011526511.1:n.242+34_242+35insTGGCCGG
XR_936204.1:n.1089+34_1089+35insTGGCCGG
XM_005259617.3:c.464+34_464+35insTGGCCGG XP_005259674.1:n.464+34_464+35insTGGCCGG
XM_011528209.2:c.242+34_242+35insTGGCCGG XP_011526511.1:n.242+34_242+35insTGGCCGG
XR_001753738.2:n.1089+34_1089+35insTGGCCGG
XR_001753739.1:n.1089+34_1089+35insTGGCCGG
XR_001753740.2:n.1089+34_1089+35insTGGCCGG
NM_000455.5:c.464+34_464+35insTGGCCGG MANE Select NP_000446.1:n.464+34_464+35insTGGCCGG