Canonical Allele Identifier: CA405691501
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 429785
ClinVar RCV Id: RCV000493888
dbSNP Id: rs1131691591

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38455704A>G , CM000681.2:g.38455704A>G GRCh38
NC_000019.9:g.38946344A>G , CM000681.1:g.38946344A>G GRCh37
NC_000019.8:g.43638184A>G NCBI36
NG_008866.1:g.27005A>G , LRG_766:g.27005A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.1744A>G ENSP00000471601.2:p.Ile582Val
ENST00000359596.8:c.1744A>G MANE Select ENSP00000352608.2:p.Ile582Val
ENST00000355481.8:c.1744A>G ENSP00000347667.3:p.Ile582Val
ENST00000359596.7:c.1744A>G ENSP00000352608.2:p.Ile582Val
ENST00000360985.7:c.1744A>G ENSP00000354254.4:p.Ile582Val
NM_000540.2:c.1744A>G , LRG_766t1:c.1744A>G NP_000531.2:p.Ile582Val
NM_001042723.1:c.1744A>G NP_001036188.1:p.Ile582Val
XM_006723317.1:c.1744A>G XP_006723380.1:p.Ile582Val
XM_006723319.1:c.1744A>G XP_006723382.1:p.Ile582Val
XM_011527204.1:c.1741A>G XP_011525506.1:p.Ile581Val
XM_011527205.1:c.1744A>G XP_011525507.1:p.Ile582Val
XM_006723317.2:c.1744A>G XP_006723380.1:p.Ile582Val
XM_006723319.2:c.1744A>G XP_006723382.1:p.Ile582Val
XM_011527205.2:c.1744A>G XP_011525507.1:p.Ile582Val
XR_001753735.1:n.1827A>G
NM_000540.3:c.1744A>G MANE Select NP_000531.2:p.Ile582Val
NM_001042723.2:c.1744A>G NP_001036188.1:p.Ile582Val