Canonical Allele Identifier: CA2584900717
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502791_38502792insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG , CM000681.2:g.38502791_38502792insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG GRCh38
NC_000019.9:g.38993431_38993432insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG , CM000681.1:g.38993431_38993432insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG GRCh37
NC_000019.8:g.43685271_43685272insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG NCBI36
NG_008866.1:g.74092_74093insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG , LRG_766:g.74092_74093insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG ENSP00000471601.2:n.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGG...
ENST00000359596.8:c.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG MANE Select ENSP00000352608.2:n.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGG...
ENST00000355481.8:c.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG ENSP00000347667.3:n.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGG...
ENST00000359596.7:c.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG ENSP00000352608.2:n.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGG...
ENST00000360985.7:c.7832+64_7832+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG ENSP00000354254.4:n.7832+64_7832+65insTAGGGGCAGGGGTAGGGGCAGGG...
ENST00000594335.5:c.1287+64_1287+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG
NM_000540.2:c.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG , LRG_766t1:c.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG NP_000531.2:n.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGG...
NM_001042723.1:c.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG NP_001036188.1:n.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCA...
XM_006723317.1:c.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG XP_006723380.1:n.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCA...
XM_006723319.1:c.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG XP_006723382.1:n.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCA...
XM_011527204.1:c.7832+64_7832+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG XP_011525506.1:n.7832+64_7832+65insTAGGGGCAGGGGTAGGGGCAGGGGCA...
XM_011527205.1:c.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG XP_011525507.1:n.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCA...
XM_006723317.2:c.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG XP_006723380.1:n.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCA...
XM_006723319.2:c.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG XP_006723382.1:n.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCA...
XM_011527205.2:c.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG XP_011525507.1:n.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCA...
XR_001753735.1:n.7918+64_7918+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG
NM_000540.3:c.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG MANE Select NP_000531.2:n.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGG...
NM_001042723.2:c.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCAGGGG NP_001036188.1:n.7835+64_7835+65insTAGGGGCAGGGGTAGGGGCAGGGGCA...