Canonical Allele Identifier: CA507245951
Gene: RYR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.39068841C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38578201C>T , CM000681.2:g.38578201C>T GRCh38
NC_000019.9:g.39068841C>T , CM000681.1:g.39068841C>T GRCh37
NC_000019.8:g.43760681C>T NCBI36
NG_008866.1:g.149502C>T , LRG_766:g.149502C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1297C>T
ENST00000688602.1:c.2694C>T
ENST00000689936.1:c.2666C>T
ENST00000359596.8:c.14361C>T MANE Select ENSP00000352608.2:p.Asp4787=
ENST00000355481.8:c.14346C>T ENSP00000347667.3:p.Asp4782=
ENST00000359596.7:c.14361C>T ENSP00000352608.2:p.Asp4787=
ENST00000360985.7:c.14343C>T ENSP00000354254.4:p.Asp4781=
NM_000540.2:c.14361C>T , LRG_766t1:c.14361C>T NP_000531.2:p.Asp4787=
NM_001042723.1:c.14346C>T NP_001036188.1:p.Asp4782=
XM_006723317.1:c.14343C>T XP_006723380.1:p.Asp4781=
XM_006723319.1:c.14328C>T XP_006723382.1:p.Asp4776=
XM_011527204.1:c.14358C>T XP_011525506.1:p.Asp4786=
XM_011527205.1:c.14274C>T XP_011525507.1:p.Asp4758=
XM_006723317.2:c.14343C>T XP_006723380.1:p.Asp4781=
XM_006723319.2:c.14328C>T XP_006723382.1:p.Asp4776=
XM_011527205.2:c.14274C>T XP_011525507.1:p.Asp4758=
NM_000540.3:c.14361C>T MANE Select NP_000531.2:p.Asp4787=
NM_001042723.2:c.14346C>T NP_001036188.1:p.Asp4782=
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