Canonical Allele Identifier: CA2335083756
Gene: RYR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38564061C= , CM000681.2:g.38564061C= GRCh38
NC_000019.9:g.39054701C= , CM000681.1:g.39054701C= GRCh37
NC_000019.8:g.43746541C= NCBI36
NG_008866.1:g.135362C= , LRG_766:g.135362C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000688602.1:c.1035-898C=
ENST00000689936.1:c.1017-898C=
ENST00000359596.8:c.12625-898C= MANE Select ENSP00000352608.2:n.12625-898C=
ENST00000355481.8:c.12610-898C= ENSP00000347667.3:n.12610-898C=
ENST00000359596.7:c.12625-898C= ENSP00000352608.2:n.12625-898C=
ENST00000360985.7:c.12607-898C= ENSP00000354254.4:n.12607-898C=
ENST00000594335.5:c.5994-898C=
NM_000540.2:c.12625-898C= , LRG_766t1:c.12625-898C= NP_000531.2:n.12625-898C=
NM_001042723.1:c.12610-898C= NP_001036188.1:n.12610-898C=
XM_006723317.1:c.12607-898C= XP_006723380.1:n.12607-898C=
XM_006723319.1:c.12592-898C= XP_006723382.1:n.12592-898C=
XM_011527204.1:c.12622-898C= XP_011525506.1:n.12622-898C=
XM_011527205.1:c.12625-898C= XP_011525507.1:n.12625-898C=
XM_006723317.2:c.12607-898C= XP_006723380.1:n.12607-898C=
XM_006723319.2:c.12592-898C= XP_006723382.1:n.12592-898C=
XM_011527205.2:c.12625-898C= XP_011525507.1:n.12625-898C=
NM_000540.3:c.12625-898C= MANE Select NP_000531.2:n.12625-898C=
NM_001042723.2:c.12610-898C= NP_001036188.1:n.12610-898C=
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