Canonical Allele Identifier: CA2335054522
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502760_38502814delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA , CM000681.2:g.38502760_38502814delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA GRCh38
NC_000019.9:g.38993400_38993454delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA , CM000681.1:g.38993400_38993454delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA GRCh37
NC_000019.8:g.43685240_43685294delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA NCBI36
NG_008866.1:g.74061_74115delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA , LRG_766:g.74061_74115delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA

Transcript Alleles

HGVS Amino-acid change
ENST00000599547.6:c.7835+33_7836-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA ENSP00000471601.2:n.7835+33_7836-66delins...
ENST00000359596.8:c.7835+33_7836-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA MANE Select ENSP00000352608.2:n.7835+33_7836-66delins...
ENST00000355481.8:c.7835+33_7836-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA ENSP00000347667.3:n.7835+33_7836-66delins...
ENST00000359596.7:c.7835+33_7836-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA ENSP00000352608.2:n.7835+33_7836-66delins...
ENST00000360985.7:c.7832+33_7833-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA ENSP00000354254.4:n.7832+33_7833-66delins...
ENST00000594335.5:c.1287+33_1288-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA
NM_000540.2:c.7835+33_7836-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA , LRG_766t1:c.7835+33_7836-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA NP_000531.2:n.7835+33_7836-66delinsGGCAGG...
NM_001042723.1:c.7835+33_7836-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA NP_001036188.1:n.7835+33_7836-66delinsGGC...
XM_006723317.1:c.7835+33_7836-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA XP_006723380.1:n.7835+33_7836-66delinsGGC...
XM_006723319.1:c.7835+33_7836-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA XP_006723382.1:n.7835+33_7836-66delinsGGC...
XM_011527204.1:c.7832+33_7833-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA XP_011525506.1:n.7832+33_7833-66delinsGGC...
XM_011527205.1:c.7835+33_7836-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA XP_011525507.1:n.7835+33_7836-66delinsGGC...
XM_006723317.2:c.7835+33_7836-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA XP_006723380.1:n.7835+33_7836-66delinsGGC...
XM_006723319.2:c.7835+33_7836-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA XP_006723382.1:n.7835+33_7836-66delinsGGC...
XM_011527205.2:c.7835+33_7836-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA XP_011525507.1:n.7835+33_7836-66delinsGGC...
XR_001753735.1:n.7918+33_7919-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA
NM_000540.3:c.7835+33_7836-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA MANE Select NP_000531.2:n.7835+33_7836-66delinsGGCAGG...
NM_001042723.2:c.7835+33_7836-66delinsGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGGAGGA NP_001036188.1:n.7835+33_7836-66delinsGGC...