Canonical Allele Identifier: CA2584899397
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38496596_38496598del , CM000681.2:g.38496596_38496598del GRCh38
NC_000019.9:g.38987236_38987238del , CM000681.1:g.38987236_38987238del GRCh37
NC_000019.8:g.43679076_43679078del NCBI36
NG_008866.1:g.67897_67899del , LRG_766:g.67897_67899del

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.6796+55_6796+57del ENSP00000471601.2:n.6796+55_6796+57del
ENST00000359596.8:c.6796+55_6796+57del MANE Select ENSP00000352608.2:n.6796+55_6796+57del
ENST00000355481.8:c.6796+55_6796+57del ENSP00000347667.3:n.6796+55_6796+57del
ENST00000359596.7:c.6796+55_6796+57del ENSP00000352608.2:n.6796+55_6796+57del
ENST00000360985.7:c.6793+55_6793+57del ENSP00000354254.4:n.6793+55_6793+57del
ENST00000594335.5:c.248+55_248+57del
NM_000540.2:c.6796+55_6796+57del , LRG_766t1:c.6796+55_6796+57del NP_000531.2:n.6796+55_6796+57del
NM_001042723.1:c.6796+55_6796+57del NP_001036188.1:n.6796+55_6796+57del
XM_006723317.1:c.6796+55_6796+57del XP_006723380.1:n.6796+55_6796+57del
XM_006723319.1:c.6796+55_6796+57del XP_006723382.1:n.6796+55_6796+57del
XM_011527204.1:c.6793+55_6793+57del XP_011525506.1:n.6793+55_6793+57del
XM_011527205.1:c.6796+55_6796+57del XP_011525507.1:n.6796+55_6796+57del
XM_006723317.2:c.6796+55_6796+57del XP_006723380.1:n.6796+55_6796+57del
XM_006723319.2:c.6796+55_6796+57del XP_006723382.1:n.6796+55_6796+57del
XM_011527205.2:c.6796+55_6796+57del XP_011525507.1:n.6796+55_6796+57del
XR_001753735.1:n.6879+55_6879+57del
NM_000540.3:c.6796+55_6796+57del MANE Select NP_000531.2:n.6796+55_6796+57del
NM_001042723.2:c.6796+55_6796+57del NP_001036188.1:n.6796+55_6796+57del