Canonical Allele Identifier: CA405682419
Gene: RYR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.39063898G>C (hg19) chr19:g.38573258G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38573258G>C , CM000681.2:g.38573258G>C GRCh38
NC_000019.9:g.39063898G>C , CM000681.1:g.39063898G>C GRCh37
NC_000019.8:g.43755738G>C NCBI36
NG_008866.1:g.144559G>C , LRG_766:g.144559G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1016G>C
ENST00000688602.1:c.2413G>C
ENST00000689936.1:c.2385G>C
ENST00000359596.8:c.14080G>C MANE Select ENSP00000352608.2:p.Glu4694Gln
ENST00000355481.8:c.14065G>C ENSP00000347667.3:p.Glu4689Gln
ENST00000359596.7:c.14080G>C ENSP00000352608.2:p.Glu4694Gln
ENST00000360985.7:c.14062G>C ENSP00000354254.4:p.Glu4688Gln
NM_000540.2:c.14080G>C , LRG_766t1:c.14080G>C NP_000531.2:p.Glu4694Gln
NM_001042723.1:c.14065G>C NP_001036188.1:p.Glu4689Gln
XM_006723317.1:c.14062G>C XP_006723380.1:p.Glu4688Gln
XM_006723319.1:c.14047G>C XP_006723382.1:p.Glu4683Gln
XM_011527204.1:c.14077G>C XP_011525506.1:p.Glu4693Gln
XM_011527205.1:c.13993G>C XP_011525507.1:p.Glu4665Gln
XM_006723317.2:c.14062G>C XP_006723380.1:p.Glu4688Gln
XM_006723319.2:c.14047G>C XP_006723382.1:p.Glu4683Gln
XM_011527205.2:c.13993G>C XP_011525507.1:p.Glu4665Gln
NM_000540.3:c.14080G>C MANE Select NP_000531.2:p.Glu4694Gln
NM_001042723.2:c.14065G>C NP_001036188.1:p.Glu4689Gln
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