Canonical Allele Identifier: CA2335054617
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502793_38502820delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG , CM000681.2:g.38502793_38502820delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG GRCh38
NC_000019.9:g.38993433_38993460delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG , CM000681.1:g.38993433_38993460delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG GRCh37
NC_000019.8:g.43685273_43685300delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG NCBI36
NG_008866.1:g.74094_74121delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG , LRG_766:g.74094_74121delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG ENSP00000471601.2:n.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAG...
ENST00000359596.8:c.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG MANE Select ENSP00000352608.2:n.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAG...
ENST00000355481.8:c.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG ENSP00000347667.3:n.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAG...
ENST00000359596.7:c.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG ENSP00000352608.2:n.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAG...
ENST00000360985.7:c.7832+66_7833-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG ENSP00000354254.4:n.7832+66_7833-60delinsAGGGGCAGGGGCAGGGGGAG...
ENST00000594335.5:c.1287+66_1288-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG
NM_000540.2:c.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG , LRG_766t1:c.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG NP_000531.2:n.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAG...
NM_001042723.1:c.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG NP_001036188.1:n.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAG...
XM_006723317.1:c.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG XP_006723380.1:n.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAG...
XM_006723319.1:c.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG XP_006723382.1:n.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAG...
XM_011527204.1:c.7832+66_7833-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG XP_011525506.1:n.7832+66_7833-60delinsAGGGGCAGGGGCAGGGGGAGGAG...
XM_011527205.1:c.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG XP_011525507.1:n.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAG...
XM_006723317.2:c.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG XP_006723380.1:n.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAG...
XM_006723319.2:c.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG XP_006723382.1:n.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAG...
XM_011527205.2:c.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG XP_011525507.1:n.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAG...
XR_001753735.1:n.7918+66_7919-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG
NM_000540.3:c.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG MANE Select NP_000531.2:n.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAG...
NM_001042723.2:c.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAGCAGGG NP_001036188.1:n.7835+66_7836-60delinsAGGGGCAGGGGCAGGGGGAGGAG...