Canonical Allele Identifier: CA507245895
Gene: RYR1 HGNC NCBI

Linked Data

gnomAD v4: 19-38578022-C-T
MyVariant Identifiers: chr19:g.39068662C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38578022C>T , CM000681.2:g.38578022C>T GRCh38
NC_000019.9:g.39068662C>T , CM000681.1:g.39068662C>T GRCh37
NC_000019.8:g.43760502C>T NCBI36
NG_008866.1:g.149323C>T , LRG_766:g.149323C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1213C>T
ENST00000688602.1:c.2610C>T
ENST00000689936.1:c.2582C>T
ENST00000359596.8:c.14277C>T MANE Select ENSP00000352608.2:p.Pro4759=
ENST00000355481.8:c.14262C>T ENSP00000347667.3:p.Pro4754=
ENST00000359596.7:c.14277C>T ENSP00000352608.2:p.Pro4759=
ENST00000360985.7:c.14259C>T ENSP00000354254.4:p.Pro4753=
NM_000540.2:c.14277C>T , LRG_766t1:c.14277C>T NP_000531.2:p.Pro4759=
NM_001042723.1:c.14262C>T NP_001036188.1:p.Pro4754=
XM_006723317.1:c.14259C>T XP_006723380.1:p.Pro4753=
XM_006723319.1:c.14244C>T XP_006723382.1:p.Pro4748=
XM_011527204.1:c.14274C>T XP_011525506.1:p.Pro4758=
XM_011527205.1:c.14190C>T XP_011525507.1:p.Pro4730=
XM_006723317.2:c.14259C>T XP_006723380.1:p.Pro4753=
XM_006723319.2:c.14244C>T XP_006723382.1:p.Pro4748=
XM_011527205.2:c.14190C>T XP_011525507.1:p.Pro4730=
NM_000540.3:c.14277C>T MANE Select NP_000531.2:p.Pro4759=
NM_001042723.2:c.14262C>T NP_001036188.1:p.Pro4754=
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