Canonical Allele Identifier: CA2584900700
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502773_38502774insTAGGGG , CM000681.2:g.38502773_38502774insTAGGGG GRCh38
NC_000019.9:g.38993413_38993414insTAGGGG , CM000681.1:g.38993413_38993414insTAGGGG GRCh37
NC_000019.8:g.43685253_43685254insTAGGGG NCBI36
NG_008866.1:g.74074_74075insTAGGGG , LRG_766:g.74074_74075insTAGGGG

Transcript Alleles

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