Canonical Allele Identifier: CA405684476
Gene: RYR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.39068615A>C (hg19) chr19:g.38577975A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38577975A>C , CM000681.2:g.38577975A>C GRCh38
NC_000019.9:g.39068615A>C , CM000681.1:g.39068615A>C GRCh37
NC_000019.8:g.43760455A>C NCBI36
NG_008866.1:g.149276A>C , LRG_766:g.149276A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1166A>C
ENST00000688602.1:c.2563A>C
ENST00000689936.1:c.2535A>C
ENST00000359596.8:c.14230A>C MANE Select ENSP00000352608.2:p.Met4744Leu
ENST00000355481.8:c.14215A>C ENSP00000347667.3:p.Met4739Leu
ENST00000359596.7:c.14230A>C ENSP00000352608.2:p.Met4744Leu
ENST00000360985.7:c.14212A>C ENSP00000354254.4:p.Met4738Leu
NM_000540.2:c.14230A>C , LRG_766t1:c.14230A>C NP_000531.2:p.Met4744Leu
NM_001042723.1:c.14215A>C NP_001036188.1:p.Met4739Leu
XM_006723317.1:c.14212A>C XP_006723380.1:p.Met4738Leu
XM_006723319.1:c.14197A>C XP_006723382.1:p.Met4733Leu
XM_011527204.1:c.14227A>C XP_011525506.1:p.Met4743Leu
XM_011527205.1:c.14143A>C XP_011525507.1:p.Met4715Leu
XM_006723317.2:c.14212A>C XP_006723380.1:p.Met4738Leu
XM_006723319.2:c.14197A>C XP_006723382.1:p.Met4733Leu
XM_011527205.2:c.14143A>C XP_011525507.1:p.Met4715Leu
NM_000540.3:c.14230A>C MANE Select NP_000531.2:p.Met4744Leu
NM_001042723.2:c.14215A>C NP_001036188.1:p.Met4739Leu
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