Canonical Allele Identifier: CA2582592136
Gene: STK11 HGNC NCBI

Linked Data

gnomAD v4: 19-1219444-G-GCGAGGGC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1219446_1219447insAGGGCCG , CM000681.2:g.1219446_1219447insAGGGCCG GRCh38
NC_000019.9:g.1219445_1219446insAGGGCCG , CM000681.1:g.1219445_1219446insAGGGCCG GRCh37
NC_000019.8:g.1170445_1170446insAGGGCCG NCBI36
NG_007460.2:g.35040_35041insAGGGCCG , LRG_319:g.35040_35041insAGGGCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.464+33_464+34insAGGGCCG ENSP00000490268.2:n.464+33_464+34insAGGGCCG
ENST00000585748.3:c.92+33_92+34insAGGGCCG ENSP00000477641.2:n.92+33_92+34insAGGGCCG
ENST00000585851.2:c.291-927_291-926insAGGGCCG ENSP00000467912.2:n.291-927_291-926insAGGGCCG
ENST00000326873.12:c.464+33_464+34insAGGGCCG MANE Select ENSP00000324856.6:n.464+33_464+34insAGGGCCG
ENST00000652231.1:c.464+33_464+34insAGGGCCG ENSP00000498804.1:n.464+33_464+34insAGGGCCG
ENST00000326873.11:c.464+33_464+34insAGGGCCG ENSP00000324856.6:n.464+33_464+34insAGGGCCG
ENST00000585851.1:c.291-927_291-926insAGGGCCG ENSP00000467912.1:n.291-927_291-926insAGGGCCG
ENST00000586243.5:c.464+33_464+34insAGGGCCG ENSP00000467240.2:n.464+33_464+34insAGGGCCG
ENST00000586358.5:n.287+33_287+34insAGGGCCG
ENST00000589152.5:n.554+33_554+34insAGGGCCG
NM_000455.4:c.464+33_464+34insAGGGCCG , LRG_319t1:c.464+33_464+34insAGGGCCG NP_000446.1:n.464+33_464+34insAGGGCCG
XM_005259617.1:c.464+33_464+34insAGGGCCG XP_005259674.1:n.464+33_464+34insAGGGCCG
XM_005259618.3:c.464+33_464+34insAGGGCCG XP_005259675.1:n.464+33_464+34insAGGGCCG
XM_011528209.1:c.242+33_242+34insAGGGCCG XP_011526511.1:n.242+33_242+34insAGGGCCG
XR_936204.1:n.1089+33_1089+34insAGGGCCG
XM_005259617.3:c.464+33_464+34insAGGGCCG XP_005259674.1:n.464+33_464+34insAGGGCCG
XM_011528209.2:c.242+33_242+34insAGGGCCG XP_011526511.1:n.242+33_242+34insAGGGCCG
XR_001753738.2:n.1089+33_1089+34insAGGGCCG
XR_001753739.1:n.1089+33_1089+34insAGGGCCG
XR_001753740.2:n.1089+33_1089+34insAGGGCCG
NM_000455.5:c.464+33_464+34insAGGGCCG MANE Select NP_000446.1:n.464+33_464+34insAGGGCCG
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