Canonical Allele Identifier: CA405684363
Gene: RYR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.39068599T>G (hg19) chr19:g.38577959T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38577959T>G , CM000681.2:g.38577959T>G GRCh38
NC_000019.9:g.39068599T>G , CM000681.1:g.39068599T>G GRCh37
NC_000019.8:g.43760439T>G NCBI36
NG_008866.1:g.149260T>G , LRG_766:g.149260T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1150T>G
ENST00000688602.1:c.2547T>G
ENST00000689936.1:c.2519T>G
ENST00000359596.8:c.14214T>G MANE Select ENSP00000352608.2:p.Ile4738Met
ENST00000355481.8:c.14199T>G ENSP00000347667.3:p.Ile4733Met
ENST00000359596.7:c.14214T>G ENSP00000352608.2:p.Ile4738Met
ENST00000360985.7:c.14196T>G ENSP00000354254.4:p.Ile4732Met
NM_000540.2:c.14214T>G , LRG_766t1:c.14214T>G NP_000531.2:p.Ile4738Met
NM_001042723.1:c.14199T>G NP_001036188.1:p.Ile4733Met
XM_006723317.1:c.14196T>G XP_006723380.1:p.Ile4732Met
XM_006723319.1:c.14181T>G XP_006723382.1:p.Ile4727Met
XM_011527204.1:c.14211T>G XP_011525506.1:p.Ile4737Met
XM_011527205.1:c.14127T>G XP_011525507.1:p.Ile4709Met
XM_006723317.2:c.14196T>G XP_006723380.1:p.Ile4732Met
XM_006723319.2:c.14181T>G XP_006723382.1:p.Ile4727Met
XM_011527205.2:c.14127T>G XP_011525507.1:p.Ile4709Met
NM_000540.3:c.14214T>G MANE Select NP_000531.2:p.Ile4738Met
NM_001042723.2:c.14199T>G NP_001036188.1:p.Ile4733Met
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