Canonical Allele Identifier: CA061034
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 945486
ClinVar RCV Id: RCV001216138 RCV002264224 RCV003398951
dbSNP Id: rs373919284
ExAC: 19:39068667 C / T
gnomAD v2: 19-39068667-C-T
gnomAD v3: 19-38578027-C-T
gnomAD v4: 19-38578027-C-T
MyVariant Identifiers: chr19:g.39068667C>T (hg19) chr19:g.38578027C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38578027C>T , CM000681.2:g.38578027C>T GRCh38
NC_000019.9:g.39068667C>T , CM000681.1:g.39068667C>T GRCh37
NC_000019.8:g.43760507C>T NCBI36
NG_008866.1:g.149328C>T , LRG_766:g.149328C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1218C>T
ENST00000688602.1:c.2615C>T
ENST00000689936.1:c.2587C>T
ENST00000359596.8:c.14282C>T MANE Select ENSP00000352608.2:p.Pro4761Leu
ENST00000355481.8:c.14267C>T ENSP00000347667.3:p.Pro4756Leu
ENST00000359596.7:c.14282C>T ENSP00000352608.2:p.Pro4761Leu
ENST00000360985.7:c.14264C>T ENSP00000354254.4:p.Pro4755Leu
NM_000540.2:c.14282C>T , LRG_766t1:c.14282C>T NP_000531.2:p.Pro4761Leu
NM_001042723.1:c.14267C>T NP_001036188.1:p.Pro4756Leu
XM_006723317.1:c.14264C>T XP_006723380.1:p.Pro4755Leu
XM_006723319.1:c.14249C>T XP_006723382.1:p.Pro4750Leu
XM_011527204.1:c.14279C>T XP_011525506.1:p.Pro4760Leu
XM_011527205.1:c.14195C>T XP_011525507.1:p.Pro4732Leu
XM_006723317.2:c.14264C>T XP_006723380.1:p.Pro4755Leu
XM_006723319.2:c.14249C>T XP_006723382.1:p.Pro4750Leu
XM_011527205.2:c.14195C>T XP_011525507.1:p.Pro4732Leu
NM_000540.3:c.14282C>T MANE Select NP_000531.2:p.Pro4761Leu
NM_001042723.2:c.14267C>T NP_001036188.1:p.Pro4756Leu
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