Canonical Allele Identifier: CA2335052732
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38499431_38499476delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG , CM000681.2:g.38499431_38499476delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG GRCh38
NC_000019.9:g.38990071_38990116delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG , CM000681.1:g.38990071_38990116delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG GRCh37
NC_000019.8:g.43681911_43681956delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG NCBI36
NG_008866.1:g.70732_70777delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG , LRG_766:g.70732_70777delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG ENSP00000471601.2:n.7027+188_7028-159delinsATCCTGGGGCTGGCGGGA...
ENST00000359596.8:c.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG MANE Select ENSP00000352608.2:n.7027+188_7028-159delinsATCCTGGGGCTGGCGGGA...
ENST00000355481.8:c.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG ENSP00000347667.3:n.7027+188_7028-159delinsATCCTGGGGCTGGCGGGA...
ENST00000359596.7:c.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG ENSP00000352608.2:n.7027+188_7028-159delinsATCCTGGGGCTGGCGGGA...
ENST00000360985.7:c.7024+188_7025-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG ENSP00000354254.4:n.7024+188_7025-159delinsATCCTGGGGCTGGCGGGA...
ENST00000594335.5:c.479+188_480-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG
NM_000540.2:c.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG , LRG_766t1:c.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG NP_000531.2:n.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGG...
NM_001042723.1:c.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG NP_001036188.1:n.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCC...
XM_006723317.1:c.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG XP_006723380.1:n.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCC...
XM_006723319.1:c.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG XP_006723382.1:n.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCC...
XM_011527204.1:c.7024+188_7025-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG XP_011525506.1:n.7024+188_7025-159delinsATCCTGGGGCTGGCGGGAGCC...
XM_011527205.1:c.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG XP_011525507.1:n.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCC...
XM_006723317.2:c.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG XP_006723380.1:n.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCC...
XM_006723319.2:c.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG XP_006723382.1:n.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCC...
XM_011527205.2:c.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG XP_011525507.1:n.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCC...
XR_001753735.1:n.7110+188_7111-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG
NM_000540.3:c.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG MANE Select NP_000531.2:n.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGG...
NM_001042723.2:c.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGG NP_001036188.1:n.7027+188_7028-159delinsATCCTGGGGCTGGCGGGAGCC...