Canonical Allele Identifier: CA405691840
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2005003
ClinVar RCV Id: RCV002828423

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38455734C>G , CM000681.2:g.38455734C>G GRCh38
NC_000019.9:g.38946374C>G , CM000681.1:g.38946374C>G GRCh37
NC_000019.8:g.43638214C>G NCBI36
NG_008866.1:g.27035C>G , LRG_766:g.27035C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.1774C>G ENSP00000471601.2:p.His592Asp
ENST00000359596.8:c.1774C>G MANE Select ENSP00000352608.2:p.His592Asp
ENST00000355481.8:c.1774C>G ENSP00000347667.3:p.His592Asp
ENST00000359596.7:c.1774C>G ENSP00000352608.2:p.His592Asp
ENST00000360985.7:c.1774C>G ENSP00000354254.4:p.His592Asp
NM_000540.2:c.1774C>G , LRG_766t1:c.1774C>G NP_000531.2:p.His592Asp
NM_001042723.1:c.1774C>G NP_001036188.1:p.His592Asp
XM_006723317.1:c.1774C>G XP_006723380.1:p.His592Asp
XM_006723319.1:c.1774C>G XP_006723382.1:p.His592Asp
XM_011527204.1:c.1771C>G XP_011525506.1:p.His591Asp
XM_011527205.1:c.1774C>G XP_011525507.1:p.His592Asp
XM_006723317.2:c.1774C>G XP_006723380.1:p.His592Asp
XM_006723319.2:c.1774C>G XP_006723382.1:p.His592Asp
XM_011527205.2:c.1774C>G XP_011525507.1:p.His592Asp
XR_001753735.1:n.1857C>G
NM_000540.3:c.1774C>G MANE Select NP_000531.2:p.His592Asp
NM_001042723.2:c.1774C>G NP_001036188.1:p.His592Asp