Canonical Allele Identifier: CA405682480
Gene: RYR1 HGNC NCBI

Linked Data

gnomAD v4: 19-38573269-C-G
MyVariant Identifiers: chr19:g.39063909C>G (hg19) chr19:g.38573269C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38573269C>G , CM000681.2:g.38573269C>G GRCh38
NC_000019.9:g.39063909C>G , CM000681.1:g.39063909C>G GRCh37
NC_000019.8:g.43755749C>G NCBI36
NG_008866.1:g.144570C>G , LRG_766:g.144570C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1027C>G
ENST00000688602.1:c.2424C>G
ENST00000689936.1:c.2396C>G
ENST00000359596.8:c.14091C>G MANE Select ENSP00000352608.2:p.Asp4697Glu
ENST00000355481.8:c.14076C>G ENSP00000347667.3:p.Asp4692Glu
ENST00000359596.7:c.14091C>G ENSP00000352608.2:p.Asp4697Glu
ENST00000360985.7:c.14073C>G ENSP00000354254.4:p.Asp4691Glu
NM_000540.2:c.14091C>G , LRG_766t1:c.14091C>G NP_000531.2:p.Asp4697Glu
NM_001042723.1:c.14076C>G NP_001036188.1:p.Asp4692Glu
XM_006723317.1:c.14073C>G XP_006723380.1:p.Asp4691Glu
XM_006723319.1:c.14058C>G XP_006723382.1:p.Asp4686Glu
XM_011527204.1:c.14088C>G XP_011525506.1:p.Asp4696Glu
XM_011527205.1:c.14004C>G XP_011525507.1:p.Asp4668Glu
XM_006723317.2:c.14073C>G XP_006723380.1:p.Asp4691Glu
XM_006723319.2:c.14058C>G XP_006723382.1:p.Asp4686Glu
XM_011527205.2:c.14004C>G XP_011525507.1:p.Asp4668Glu
NM_000540.3:c.14091C>G MANE Select NP_000531.2:p.Asp4697Glu
NM_001042723.2:c.14076C>G NP_001036188.1:p.Asp4692Glu
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