Canonical Allele Identifier: CA405679823
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3157343
ClinVar RCV Id: RCV004447186
MyVariant Identifiers: chr19:g.38937193A>G (hg19) chr19:g.38446553A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38446553A>G , CM000681.2:g.38446553A>G GRCh38
NC_000019.9:g.38937193A>G , CM000681.1:g.38937193A>G GRCh37
NC_000019.8:g.43629033A>G NCBI36
NG_008866.1:g.17854A>G , LRG_766:g.17854A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.713A>G ENSP00000471601.2:p.Asp238Gly
ENST00000359596.8:c.713A>G MANE Select ENSP00000352608.2:p.Asp238Gly
ENST00000355481.8:c.713A>G ENSP00000347667.3:p.Asp238Gly
ENST00000359596.7:c.713A>G ENSP00000352608.2:p.Asp238Gly
ENST00000360985.7:c.713A>G ENSP00000354254.4:p.Asp238Gly
NM_000540.2:c.713A>G , LRG_766t1:c.713A>G NP_000531.2:p.Asp238Gly
NM_001042723.1:c.713A>G NP_001036188.1:p.Asp238Gly
XM_006723317.1:c.713A>G XP_006723380.1:p.Asp238Gly
XM_006723319.1:c.713A>G XP_006723382.1:p.Asp238Gly
XM_011527204.1:c.713A>G XP_011525506.1:p.Asp238Gly
XM_011527205.1:c.713A>G XP_011525507.1:p.Asp238Gly
XM_006723317.2:c.713A>G XP_006723380.1:p.Asp238Gly
XM_006723319.2:c.713A>G XP_006723382.1:p.Asp238Gly
XM_011527205.2:c.713A>G XP_011525507.1:p.Asp238Gly
XR_001753735.1:n.796A>G
NM_000540.3:c.713A>G MANE Select NP_000531.2:p.Asp238Gly
NM_001042723.2:c.713A>G NP_001036188.1:p.Asp238Gly
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