Canonical Allele Identifier: CA633066298
Gene: RYR1 HGNC NCBI

Linked Data

dbSNP Id: rs1491128509

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502803_38502804insGAGGGGGAGGGGGAGGGG , CM000681.2:g.38502803_38502804insGAGGGGGAGGGGGAGGGG GRCh38
NC_000019.9:g.38993443_38993444insGAGGGGGAGGGGGAGGGG , CM000681.1:g.38993443_38993444insGAGGGGGAGGGGGAGGGG GRCh37
NC_000019.8:g.43685283_43685284insGAGGGGGAGGGGGAGGGG NCBI36
NG_008866.1:g.74104_74105insGAGGGGGAGGGGGAGGGG , LRG_766:g.74104_74105insGAGGGGGAGGGGGAGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7836-77_7836-76insGAGGGGGAGGGGGAGGGG ENSP00000471601.2:n.7836-77_7836-76insGAGGGGGAGGGGGAGGGG
ENST00000359596.8:c.7836-77_7836-76insGAGGGGGAGGGGGAGGGG MANE Select ENSP00000352608.2:n.7836-77_7836-76insGAGGGGGAGGGGGAGGGG
ENST00000355481.8:c.7836-77_7836-76insGAGGGGGAGGGGGAGGGG ENSP00000347667.3:n.7836-77_7836-76insGAGGGGGAGGGGGAGGGG
ENST00000359596.7:c.7836-77_7836-76insGAGGGGGAGGGGGAGGGG ENSP00000352608.2:n.7836-77_7836-76insGAGGGGGAGGGGGAGGGG
ENST00000360985.7:c.7833-77_7833-76insGAGGGGGAGGGGGAGGGG ENSP00000354254.4:n.7833-77_7833-76insGAGGGGGAGGGGGAGGGG
ENST00000594335.5:c.1288-77_1288-76insGAGGGGGAGGGGGAGGGG
NM_000540.2:c.7836-77_7836-76insGAGGGGGAGGGGGAGGGG , LRG_766t1:c.7836-77_7836-76insGAGGGGGAGGGGGAGGGG NP_000531.2:n.7836-77_7836-76insGAGGGGGAGGGGGAGGGG
NM_001042723.1:c.7836-77_7836-76insGAGGGGGAGGGGGAGGGG NP_001036188.1:n.7836-77_7836-76insGAGGGGGAGGGGGAGGGG
XM_006723317.1:c.7836-77_7836-76insGAGGGGGAGGGGGAGGGG XP_006723380.1:n.7836-77_7836-76insGAGGGGGAGGGGGAGGGG
XM_006723319.1:c.7836-77_7836-76insGAGGGGGAGGGGGAGGGG XP_006723382.1:n.7836-77_7836-76insGAGGGGGAGGGGGAGGGG
XM_011527204.1:c.7833-77_7833-76insGAGGGGGAGGGGGAGGGG XP_011525506.1:n.7833-77_7833-76insGAGGGGGAGGGGGAGGGG
XM_011527205.1:c.7836-77_7836-76insGAGGGGGAGGGGGAGGGG XP_011525507.1:n.7836-77_7836-76insGAGGGGGAGGGGGAGGGG
XM_006723317.2:c.7836-77_7836-76insGAGGGGGAGGGGGAGGGG XP_006723380.1:n.7836-77_7836-76insGAGGGGGAGGGGGAGGGG
XM_006723319.2:c.7836-77_7836-76insGAGGGGGAGGGGGAGGGG XP_006723382.1:n.7836-77_7836-76insGAGGGGGAGGGGGAGGGG
XM_011527205.2:c.7836-77_7836-76insGAGGGGGAGGGGGAGGGG XP_011525507.1:n.7836-77_7836-76insGAGGGGGAGGGGGAGGGG
XR_001753735.1:n.7919-77_7919-76insGAGGGGGAGGGGGAGGGG
NM_000540.3:c.7836-77_7836-76insGAGGGGGAGGGGGAGGGG MANE Select NP_000531.2:n.7836-77_7836-76insGAGGGGGAGGGGGAGGGG
NM_001042723.2:c.7836-77_7836-76insGAGGGGGAGGGGGAGGGG NP_001036188.1:n.7836-77_7836-76insGAGGGGGAGGGGGAGGGG