Canonical Allele Identifier: CA073912
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 329090
dbSNP Id: rs199738299

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38516167A>G , CM000681.2:g.38516167A>G GRCh38
NC_000019.9:g.39006807A>G , CM000681.1:g.39006807A>G GRCh37
NC_000019.8:g.43698647A>G NCBI36
NG_008866.1:g.87468A>G , LRG_766:g.87468A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.9574A>G ENSP00000471601.2:n.9574A>G
ENST00000359596.8:c.9635A>G MANE Select ENSP00000352608.2:p.Glu3212Gly
ENST00000355481.8:c.9635A>G ENSP00000347667.3:p.Glu3212Gly
ENST00000359596.7:c.9635A>G ENSP00000352608.2:p.Glu3212Gly
ENST00000360985.7:c.9632A>G ENSP00000354254.4:p.Glu3211Gly
ENST00000594335.5:c.3037A>G
ENST00000599547.5:c.442A>G
NM_000540.2:c.9635A>G , LRG_766t1:c.9635A>G NP_000531.2:p.Glu3212Gly
NM_001042723.1:c.9635A>G NP_001036188.1:p.Glu3212Gly
XM_006723317.1:c.9635A>G XP_006723380.1:p.Glu3212Gly
XM_006723319.1:c.9635A>G XP_006723382.1:p.Glu3212Gly
XM_011527204.1:c.9632A>G XP_011525506.1:p.Glu3211Gly
XM_011527205.1:c.9635A>G XP_011525507.1:p.Glu3212Gly
XM_006723317.2:c.9635A>G XP_006723380.1:p.Glu3212Gly
XM_006723319.2:c.9635A>G XP_006723382.1:p.Glu3212Gly
XM_011527205.2:c.9635A>G XP_011525507.1:p.Glu3212Gly
XR_001753735.1:n.9668A>G
NM_000540.3:c.9635A>G MANE Select NP_000531.2:p.Glu3212Gly
NM_001042723.2:c.9635A>G NP_001036188.1:p.Glu3212Gly