Canonical Allele Identifier: CA405655013
Gene: RYR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.38976692C>A (hg19) chr19:g.38486052C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38486052C>A , CM000681.2:g.38486052C>A GRCh38
NC_000019.9:g.38976692C>A , CM000681.1:g.38976692C>A GRCh37
NC_000019.8:g.43668532C>A NCBI36
NG_008866.1:g.57353C>A , LRG_766:g.57353C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.5397C>A ENSP00000471601.2:p.Ser1799Arg
ENST00000359596.8:c.5397C>A MANE Select ENSP00000352608.2:p.Ser1799Arg
ENST00000355481.8:c.5397C>A ENSP00000347667.3:p.Ser1799Arg
ENST00000359596.7:c.5397C>A ENSP00000352608.2:p.Ser1799Arg
ENST00000360985.7:c.5394C>A ENSP00000354254.4:p.Ser1798Arg
NM_000540.2:c.5397C>A , LRG_766t1:c.5397C>A NP_000531.2:p.Ser1799Arg
NM_001042723.1:c.5397C>A NP_001036188.1:p.Ser1799Arg
XM_006723317.1:c.5397C>A XP_006723380.1:p.Ser1799Arg
XM_006723319.1:c.5397C>A XP_006723382.1:p.Ser1799Arg
XM_011527204.1:c.5394C>A XP_011525506.1:p.Ser1798Arg
XM_011527205.1:c.5397C>A XP_011525507.1:p.Ser1799Arg
XM_006723317.2:c.5397C>A XP_006723380.1:p.Ser1799Arg
XM_006723319.2:c.5397C>A XP_006723382.1:p.Ser1799Arg
XM_011527205.2:c.5397C>A XP_011525507.1:p.Ser1799Arg
XR_001753735.1:n.5480C>A
NM_000540.3:c.5397C>A MANE Select NP_000531.2:p.Ser1799Arg
NM_001042723.2:c.5397C>A NP_001036188.1:p.Ser1799Arg
Search 100 bp 5'
Search 100 bp 3'