Canonical Allele Identifier: CA405682342
Gene: RYR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.39063886A>T (hg19) chr19:g.38573246A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38573246A>T , CM000681.2:g.38573246A>T GRCh38
NC_000019.9:g.39063886A>T , CM000681.1:g.39063886A>T GRCh37
NC_000019.8:g.43755726A>T NCBI36
NG_008866.1:g.144547A>T , LRG_766:g.144547A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1004A>T
ENST00000688602.1:c.2401A>T
ENST00000689936.1:c.2373A>T
ENST00000359596.8:c.14068A>T MANE Select ENSP00000352608.2:p.Thr4690Ser
ENST00000355481.8:c.14053A>T ENSP00000347667.3:p.Thr4685Ser
ENST00000359596.7:c.14068A>T ENSP00000352608.2:p.Thr4690Ser
ENST00000360985.7:c.14050A>T ENSP00000354254.4:p.Thr4684Ser
NM_000540.2:c.14068A>T , LRG_766t1:c.14068A>T NP_000531.2:p.Thr4690Ser
NM_001042723.1:c.14053A>T NP_001036188.1:p.Thr4685Ser
XM_006723317.1:c.14050A>T XP_006723380.1:p.Thr4684Ser
XM_006723319.1:c.14035A>T XP_006723382.1:p.Thr4679Ser
XM_011527204.1:c.14065A>T XP_011525506.1:p.Thr4689Ser
XM_011527205.1:c.13981A>T XP_011525507.1:p.Thr4661Ser
XM_006723317.2:c.14050A>T XP_006723380.1:p.Thr4684Ser
XM_006723319.2:c.14035A>T XP_006723382.1:p.Thr4679Ser
XM_011527205.2:c.13981A>T XP_011525507.1:p.Thr4661Ser
NM_000540.3:c.14068A>T MANE Select NP_000531.2:p.Thr4690Ser
NM_001042723.2:c.14053A>T NP_001036188.1:p.Thr4685Ser
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