Canonical Allele Identifier: CA024289
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159838
dbSNP Id: rs61586345

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38455445C>G , CM000681.2:g.38455445C>G GRCh38
NC_000019.9:g.38946085C>G , CM000681.1:g.38946085C>G GRCh37
NC_000019.8:g.43637925C>G NCBI36
NG_008866.1:g.26746C>G , LRG_766:g.26746C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.1577-6C>G ENSP00000471601.2:n.1577-6C>G
ENST00000359596.8:c.1577-6C>G MANE Select ENSP00000352608.2:n.1577-6C>G
ENST00000355481.8:c.1577-6C>G ENSP00000347667.3:n.1577-6C>G
ENST00000359596.7:c.1577-6C>G ENSP00000352608.2:n.1577-6C>G
ENST00000360985.7:c.1577-6C>G ENSP00000354254.4:n.1577-6C>G
NM_000540.2:c.1577-6C>G , LRG_766t1:c.1577-6C>G NP_000531.2:n.1577-6C>G
NM_001042723.1:c.1577-6C>G NP_001036188.1:n.1577-6C>G
XM_006723317.1:c.1577-6C>G XP_006723380.1:n.1577-6C>G
XM_006723319.1:c.1577-6C>G XP_006723382.1:n.1577-6C>G
XM_011527204.1:c.1574-6C>G XP_011525506.1:n.1574-6C>G
XM_011527205.1:c.1577-6C>G XP_011525507.1:n.1577-6C>G
XM_006723317.2:c.1577-6C>G XP_006723380.1:n.1577-6C>G
XM_006723319.2:c.1577-6C>G XP_006723382.1:n.1577-6C>G
XM_011527205.2:c.1577-6C>G XP_011525507.1:n.1577-6C>G
XR_001753735.1:n.1660-6C>G
NM_000540.3:c.1577-6C>G MANE Select NP_000531.2:n.1577-6C>G
NM_001042723.2:c.1577-6C>G NP_001036188.1:n.1577-6C>G