Canonical Allele Identifier: CA2335054670
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502808_38502829delinsGGGAGGAGCAGGGGCAGGGGCA , CM000681.2:g.38502808_38502829delinsGGGAGGAGCAGGGGCAGGGGCA GRCh38
NC_000019.9:g.38993448_38993469delinsGGGAGGAGCAGGGGCAGGGGCA , CM000681.1:g.38993448_38993469delinsGGGAGGAGCAGGGGCAGGGGCA GRCh37
NC_000019.8:g.43685288_43685309delinsGGGAGGAGCAGGGGCAGGGGCA NCBI36
NG_008866.1:g.74109_74130delinsGGGAGGAGCAGGGGCAGGGGCA , LRG_766:g.74109_74130delinsGGGAGGAGCAGGGGCAGGGGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA ENSP00000471601.2:n.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGG...
ENST00000359596.8:c.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA MANE Select ENSP00000352608.2:n.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGG...
ENST00000355481.8:c.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA ENSP00000347667.3:n.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGG...
ENST00000359596.7:c.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA ENSP00000352608.2:n.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGG...
ENST00000360985.7:c.7833-72_7833-51delinsGGGAGGAGCAGGGGCAGGGGCA ENSP00000354254.4:n.7833-72_7833-51delinsGGGAGGAGCAGGGGCAGGGG...
ENST00000594335.5:c.1288-72_1288-51delinsGGGAGGAGCAGGGGCAGGGGCA
NM_000540.2:c.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA , LRG_766t1:c.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA NP_000531.2:n.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA
NM_001042723.1:c.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA NP_001036188.1:n.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA
XM_006723317.1:c.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA XP_006723380.1:n.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA
XM_006723319.1:c.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA XP_006723382.1:n.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA
XM_011527204.1:c.7833-72_7833-51delinsGGGAGGAGCAGGGGCAGGGGCA XP_011525506.1:n.7833-72_7833-51delinsGGGAGGAGCAGGGGCAGGGGCA
XM_011527205.1:c.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA XP_011525507.1:n.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA
XM_006723317.2:c.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA XP_006723380.1:n.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA
XM_006723319.2:c.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA XP_006723382.1:n.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA
XM_011527205.2:c.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA XP_011525507.1:n.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA
XR_001753735.1:n.7919-72_7919-51delinsGGGAGGAGCAGGGGCAGGGGCA
NM_000540.3:c.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA MANE Select NP_000531.2:n.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA
NM_001042723.2:c.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA NP_001036188.1:n.7836-72_7836-51delinsGGGAGGAGCAGGGGCAGGGGCA