Canonical Allele Identifier: CA405681820
Gene: RYR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.39063827T>G (hg19) chr19:g.38573187T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38573187T>G , CM000681.2:g.38573187T>G GRCh38
NC_000019.9:g.39063827T>G , CM000681.1:g.39063827T>G GRCh37
NC_000019.8:g.43755667T>G NCBI36
NG_008866.1:g.144488T>G , LRG_766:g.144488T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.945T>G
ENST00000688602.1:c.2342T>G
ENST00000689936.1:c.2314T>G
ENST00000359596.8:c.14009T>G MANE Select ENSP00000352608.2:p.Val4670Gly
ENST00000355481.8:c.13994T>G ENSP00000347667.3:p.Val4665Gly
ENST00000359596.7:c.14009T>G ENSP00000352608.2:p.Val4670Gly
ENST00000360985.7:c.13991T>G ENSP00000354254.4:p.Val4664Gly
NM_000540.2:c.14009T>G , LRG_766t1:c.14009T>G NP_000531.2:p.Val4670Gly
NM_001042723.1:c.13994T>G NP_001036188.1:p.Val4665Gly
XM_006723317.1:c.13991T>G XP_006723380.1:p.Val4664Gly
XM_006723319.1:c.13976T>G XP_006723382.1:p.Val4659Gly
XM_011527204.1:c.14006T>G XP_011525506.1:p.Val4669Gly
XM_011527205.1:c.13922T>G XP_011525507.1:p.Val4641Gly
XM_006723317.2:c.13991T>G XP_006723380.1:p.Val4664Gly
XM_006723319.2:c.13976T>G XP_006723382.1:p.Val4659Gly
XM_011527205.2:c.13922T>G XP_011525507.1:p.Val4641Gly
NM_000540.3:c.14009T>G MANE Select NP_000531.2:p.Val4670Gly
NM_001042723.2:c.13994T>G NP_001036188.1:p.Val4665Gly
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