Canonical Allele Identifier: CA2335054458
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502729_38502734delinsTGGAGC , CM000681.2:g.38502729_38502734delinsTGGAGC GRCh38
NC_000019.9:g.38993369_38993374delinsTGGAGC , CM000681.1:g.38993369_38993374delinsTGGAGC GRCh37
NC_000019.8:g.43685209_43685214delinsTGGAGC NCBI36
NG_008866.1:g.74030_74035delinsTGGAGC , LRG_766:g.74030_74035delinsTGGAGC

Transcript Alleles

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