Canonical Allele Identifier: CA024494
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133144
dbSNP Id: rs193922781

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38485838C>T , CM000681.2:g.38485838C>T GRCh38
NC_000019.9:g.38976478C>T , CM000681.1:g.38976478C>T GRCh37
NC_000019.8:g.43668318C>T NCBI36
NG_008866.1:g.57139C>T , LRG_766:g.57139C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.5183C>T ENSP00000471601.2:p.Ser1728Phe
ENST00000359596.8:c.5183C>T MANE Select ENSP00000352608.2:p.Ser1728Phe
ENST00000355481.8:c.5183C>T ENSP00000347667.3:p.Ser1728Phe
ENST00000359596.7:c.5183C>T ENSP00000352608.2:p.Ser1728Phe
ENST00000360985.7:c.5180C>T ENSP00000354254.4:p.Ser1727Phe
NM_000540.2:c.5183C>T , LRG_766t1:c.5183C>T NP_000531.2:p.Ser1728Phe
NM_001042723.1:c.5183C>T NP_001036188.1:p.Ser1728Phe
XM_006723317.1:c.5183C>T XP_006723380.1:p.Ser1728Phe
XM_006723319.1:c.5183C>T XP_006723382.1:p.Ser1728Phe
XM_011527204.1:c.5180C>T XP_011525506.1:p.Ser1727Phe
XM_011527205.1:c.5183C>T XP_011525507.1:p.Ser1728Phe
XM_006723317.2:c.5183C>T XP_006723380.1:p.Ser1728Phe
XM_006723319.2:c.5183C>T XP_006723382.1:p.Ser1728Phe
XM_011527205.2:c.5183C>T XP_011525507.1:p.Ser1728Phe
XR_001753735.1:n.5266C>T
NM_000540.3:c.5183C>T MANE Select NP_000531.2:p.Ser1728Phe
NM_001042723.2:c.5183C>T NP_001036188.1:p.Ser1728Phe