Canonical Allele Identifier: CA2573156323
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1667713
ClinVar RCV Id: RCV002195829
dbSNP Id: rs2145889353
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38578213G>A , CM000681.2:g.38578213G>A GRCh38
NC_000019.9:g.39068853G>A , CM000681.1:g.39068853G>A GRCh37
NC_000019.8:g.43760693G>A NCBI36
NG_008866.1:g.149514G>A , LRG_766:g.149514G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1300+9G>A
ENST00000688602.1:c.2697+9G>A
ENST00000689936.1:c.2669+9G>A
ENST00000359596.8:c.14364+9G>A MANE Select ENSP00000352608.2:n.14364+9G>A
ENST00000355481.8:c.14349+9G>A ENSP00000347667.3:n.14349+9G>A
ENST00000359596.7:c.14364+9G>A ENSP00000352608.2:n.14364+9G>A
ENST00000360985.7:c.14346+9G>A ENSP00000354254.4:n.14346+9G>A
NM_000540.2:c.14364+9G>A , LRG_766t1:c.14364+9G>A NP_000531.2:n.14364+9G>A
NM_001042723.1:c.14349+9G>A NP_001036188.1:n.14349+9G>A
XM_006723317.1:c.14346+9G>A XP_006723380.1:n.14346+9G>A
XM_006723319.1:c.14331+9G>A XP_006723382.1:n.14331+9G>A
XM_011527204.1:c.14361+9G>A XP_011525506.1:n.14361+9G>A
XM_011527205.1:c.14277+9G>A XP_011525507.1:n.14277+9G>A
XM_006723317.2:c.14346+9G>A XP_006723380.1:n.14346+9G>A
XM_006723319.2:c.14331+9G>A XP_006723382.1:n.14331+9G>A
XM_011527205.2:c.14277+9G>A XP_011525507.1:n.14277+9G>A
NM_000540.3:c.14364+9G>A MANE Select NP_000531.2:n.14364+9G>A
NM_001042723.2:c.14349+9G>A NP_001036188.1:n.14349+9G>A
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