Canonical Allele Identifier: CA2584900648
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502753_38502754insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG , CM000681.2:g.38502753_38502754insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG GRCh38
NC_000019.9:g.38993393_38993394insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG , CM000681.1:g.38993393_38993394insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG GRCh37
NC_000019.8:g.43685233_43685234insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG NCBI36
NG_008866.1:g.74054_74055insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG , LRG_766:g.74054_74055insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG ENSP00000471601.2:n.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGG...
ENST00000359596.8:c.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG MANE Select ENSP00000352608.2:n.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGG...
ENST00000355481.8:c.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG ENSP00000347667.3:n.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGG...
ENST00000359596.7:c.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG ENSP00000352608.2:n.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGG...
ENST00000360985.7:c.7832+26_7832+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG ENSP00000354254.4:n.7832+26_7832+27insAGCGGGGCAGGCTTCAGGGTGGG...
ENST00000594335.5:c.1287+26_1287+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG
NM_000540.2:c.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG , LRG_766t1:c.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG NP_000531.2:n.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGG...
NM_001042723.1:c.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG NP_001036188.1:n.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCA...
XM_006723317.1:c.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG XP_006723380.1:n.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCA...
XM_006723319.1:c.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG XP_006723382.1:n.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCA...
XM_011527204.1:c.7832+26_7832+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG XP_011525506.1:n.7832+26_7832+27insAGCGGGGCAGGCTTCAGGGTGGGGCA...
XM_011527205.1:c.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG XP_011525507.1:n.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCA...
XM_006723317.2:c.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG XP_006723380.1:n.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCA...
XM_006723319.2:c.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG XP_006723382.1:n.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCA...
XM_011527205.2:c.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG XP_011525507.1:n.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCA...
XR_001753735.1:n.7918+26_7918+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG
NM_000540.3:c.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG MANE Select NP_000531.2:n.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGG...
NM_001042723.2:c.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGG NP_001036188.1:n.7835+26_7835+27insAGCGGGGCAGGCTTCAGGGTGGGGCA...