Canonical Allele Identifier: CA507245904
Gene: RYR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.39068674A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38578034A>T , CM000681.2:g.38578034A>T GRCh38
NC_000019.9:g.39068674A>T , CM000681.1:g.39068674A>T GRCh37
NC_000019.8:g.43760514A>T NCBI36
NG_008866.1:g.149335A>T , LRG_766:g.149335A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1225A>T
ENST00000688602.1:c.2622A>T
ENST00000689936.1:c.2594A>T
ENST00000359596.8:c.14289A>T MANE Select ENSP00000352608.2:p.Pro4763=
ENST00000355481.8:c.14274A>T ENSP00000347667.3:p.Pro4758=
ENST00000359596.7:c.14289A>T ENSP00000352608.2:p.Pro4763=
ENST00000360985.7:c.14271A>T ENSP00000354254.4:p.Pro4757=
NM_000540.2:c.14289A>T , LRG_766t1:c.14289A>T NP_000531.2:p.Pro4763=
NM_001042723.1:c.14274A>T NP_001036188.1:p.Pro4758=
XM_006723317.1:c.14271A>T XP_006723380.1:p.Pro4757=
XM_006723319.1:c.14256A>T XP_006723382.1:p.Pro4752=
XM_011527204.1:c.14286A>T XP_011525506.1:p.Pro4762=
XM_011527205.1:c.14202A>T XP_011525507.1:p.Pro4734=
XM_006723317.2:c.14271A>T XP_006723380.1:p.Pro4757=
XM_006723319.2:c.14256A>T XP_006723382.1:p.Pro4752=
XM_011527205.2:c.14202A>T XP_011525507.1:p.Pro4734=
NM_000540.3:c.14289A>T MANE Select NP_000531.2:p.Pro4763=
NM_001042723.2:c.14274A>T NP_001036188.1:p.Pro4758=
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