Canonical Allele Identifier: CA405668048
Gene: RYR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.38990347C>A (hg19) chr19:g.38499707C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38499707C>A , CM000681.2:g.38499707C>A GRCh38
NC_000019.9:g.38990347C>A , CM000681.1:g.38990347C>A GRCh37
NC_000019.8:g.43682187C>A NCBI36
NG_008866.1:g.71008C>A , LRG_766:g.71008C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7100C>A ENSP00000471601.2:p.Ala2367Asp
ENST00000359596.8:c.7100C>A MANE Select ENSP00000352608.2:p.Ala2367Asp
ENST00000355481.8:c.7100C>A ENSP00000347667.3:p.Ala2367Asp
ENST00000359596.7:c.7100C>A ENSP00000352608.2:p.Ala2367Asp
ENST00000360985.7:c.7097C>A ENSP00000354254.4:p.Ala2366Asp
ENST00000594335.5:c.552C>A
NM_000540.2:c.7100C>A , LRG_766t1:c.7100C>A NP_000531.2:p.Ala2367Asp
NM_001042723.1:c.7100C>A NP_001036188.1:p.Ala2367Asp
XM_006723317.1:c.7100C>A XP_006723380.1:p.Ala2367Asp
XM_006723319.1:c.7100C>A XP_006723382.1:p.Ala2367Asp
XM_011527204.1:c.7097C>A XP_011525506.1:p.Ala2366Asp
XM_011527205.1:c.7100C>A XP_011525507.1:p.Ala2367Asp
XM_006723317.2:c.7100C>A XP_006723380.1:p.Ala2367Asp
XM_006723319.2:c.7100C>A XP_006723382.1:p.Ala2367Asp
XM_011527205.2:c.7100C>A XP_011525507.1:p.Ala2367Asp
XR_001753735.1:n.7183C>A
NM_000540.3:c.7100C>A MANE Select NP_000531.2:p.Ala2367Asp
NM_001042723.2:c.7100C>A NP_001036188.1:p.Ala2367Asp
Search 100 bp 5'
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