Canonical Allele Identifier: CA2335074484
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38543707C= , CM000681.2:g.38543707C= GRCh38
NC_000019.9:g.39034347C= , CM000681.1:g.39034347C= GRCh37
NC_000019.8:g.43726187C= NCBI36
NG_008866.1:g.115008C= , LRG_766:g.115008C=

Transcript Alleles

HGVS Amino-acid change
ENST00000688602.1:c.317+47C=
ENST00000689936.1:c.299+47C=
ENST00000359596.8:c.11907+47C= MANE Select ENSP00000352608.2:n.11907+47C=
ENST00000355481.8:c.11892+47C= ENSP00000347667.3:n.11892+47C=
ENST00000359596.7:c.11907+47C= ENSP00000352608.2:n.11907+47C=
ENST00000360985.7:c.11889+47C= ENSP00000354254.4:n.11889+47C=
ENST00000593322.1:c.516+47C=
ENST00000594335.5:c.5276+47C=
NM_000540.2:c.11907+47C= , LRG_766t1:c.11907+47C= NP_000531.2:n.11907+47C=
NM_001042723.1:c.11892+47C= NP_001036188.1:n.11892+47C=
XM_006723317.1:c.11889+47C= XP_006723380.1:n.11889+47C=
XM_006723319.1:c.11874+47C= XP_006723382.1:n.11874+47C=
XM_011527204.1:c.11904+47C= XP_011525506.1:n.11904+47C=
XM_011527205.1:c.11907+47C= XP_011525507.1:n.11907+47C=
XM_006723317.2:c.11889+47C= XP_006723380.1:n.11889+47C=
XM_006723319.2:c.11874+47C= XP_006723382.1:n.11874+47C=
XM_011527205.2:c.11907+47C= XP_011525507.1:n.11907+47C=
NM_000540.3:c.11907+47C= MANE Select NP_000531.2:n.11907+47C=
NM_001042723.2:c.11892+47C= NP_001036188.1:n.11892+47C=