Canonical Allele Identifier: CA2584900701
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502773_38502774insGAGGGG , CM000681.2:g.38502773_38502774insGAGGGG GRCh38
NC_000019.9:g.38993413_38993414insGAGGGG , CM000681.1:g.38993413_38993414insGAGGGG GRCh37
NC_000019.8:g.43685253_43685254insGAGGGG NCBI36
NG_008866.1:g.74074_74075insGAGGGG , LRG_766:g.74074_74075insGAGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7835+46_7835+47insGAGGGG ENSP00000471601.2:n.7835+46_7835+47insGAGGGG
ENST00000359596.8:c.7835+46_7835+47insGAGGGG MANE Select ENSP00000352608.2:n.7835+46_7835+47insGAGGGG
ENST00000355481.8:c.7835+46_7835+47insGAGGGG ENSP00000347667.3:n.7835+46_7835+47insGAGGGG
ENST00000359596.7:c.7835+46_7835+47insGAGGGG ENSP00000352608.2:n.7835+46_7835+47insGAGGGG
ENST00000360985.7:c.7832+46_7832+47insGAGGGG ENSP00000354254.4:n.7832+46_7832+47insGAGGGG
ENST00000594335.5:c.1287+46_1287+47insGAGGGG
NM_000540.2:c.7835+46_7835+47insGAGGGG , LRG_766t1:c.7835+46_7835+47insGAGGGG NP_000531.2:n.7835+46_7835+47insGAGGGG
NM_001042723.1:c.7835+46_7835+47insGAGGGG NP_001036188.1:n.7835+46_7835+47insGAGGGG
XM_006723317.1:c.7835+46_7835+47insGAGGGG XP_006723380.1:n.7835+46_7835+47insGAGGGG
XM_006723319.1:c.7835+46_7835+47insGAGGGG XP_006723382.1:n.7835+46_7835+47insGAGGGG
XM_011527204.1:c.7832+46_7832+47insGAGGGG XP_011525506.1:n.7832+46_7832+47insGAGGGG
XM_011527205.1:c.7835+46_7835+47insGAGGGG XP_011525507.1:n.7835+46_7835+47insGAGGGG
XM_006723317.2:c.7835+46_7835+47insGAGGGG XP_006723380.1:n.7835+46_7835+47insGAGGGG
XM_006723319.2:c.7835+46_7835+47insGAGGGG XP_006723382.1:n.7835+46_7835+47insGAGGGG
XM_011527205.2:c.7835+46_7835+47insGAGGGG XP_011525507.1:n.7835+46_7835+47insGAGGGG
XR_001753735.1:n.7918+46_7918+47insGAGGGG
NM_000540.3:c.7835+46_7835+47insGAGGGG MANE Select NP_000531.2:n.7835+46_7835+47insGAGGGG
NM_001042723.2:c.7835+46_7835+47insGAGGGG NP_001036188.1:n.7835+46_7835+47insGAGGGG