Canonical Allele Identifier: CA995707718
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38441031_38441041del , CM000681.2:g.38441031_38441041del GRCh38
NC_000019.9:g.38931671_38931681del , CM000681.1:g.38931671_38931681del GRCh37
NC_000019.8:g.43623511_43623521del NCBI36
NG_008866.1:g.12332_12342del , LRG_766:g.12332_12342del

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.165+167_165+177del ENSP00000471601.2:n.165+167_165+177del
ENST00000359596.8:c.165+167_165+177del MANE Select ENSP00000352608.2:n.165+167_165+177del
ENST00000355481.8:c.165+167_165+177del ENSP00000347667.3:n.165+167_165+177del
ENST00000359596.7:c.165+167_165+177del ENSP00000352608.2:n.165+167_165+177del
ENST00000360985.7:c.165+167_165+177del ENSP00000354254.4:n.165+167_165+177del
NM_000540.2:c.165+167_165+177del , LRG_766t1:c.165+167_165+177del NP_000531.2:n.165+167_165+177del
NM_001042723.1:c.165+167_165+177del NP_001036188.1:n.165+167_165+177del
XM_006723317.1:c.165+167_165+177del XP_006723380.1:n.165+167_165+177del
XM_006723319.1:c.165+167_165+177del XP_006723382.1:n.165+167_165+177del
XM_011527204.1:c.165+167_165+177del XP_011525506.1:n.165+167_165+177del
XM_011527205.1:c.165+167_165+177del XP_011525507.1:n.165+167_165+177del
XM_006723317.2:c.165+167_165+177del XP_006723380.1:n.165+167_165+177del
XM_006723319.2:c.165+167_165+177del XP_006723382.1:n.165+167_165+177del
XM_011527205.2:c.165+167_165+177del XP_011525507.1:n.165+167_165+177del
XR_001753735.1:n.248+167_248+177del
NM_000540.3:c.165+167_165+177del MANE Select NP_000531.2:n.165+167_165+177del
NM_001042723.2:c.165+167_165+177del NP_001036188.1:n.165+167_165+177del