Canonical Allele Identifier: CA2814345963
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38496603_38496604del , CM000681.2:g.38496603_38496604del GRCh38
NC_000019.9:g.38987243_38987244del , CM000681.1:g.38987243_38987244del GRCh37
NC_000019.8:g.43679083_43679084del NCBI36
NG_008866.1:g.67904_67905del , LRG_766:g.67904_67905del

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.6796+62_6796+63del ENSP00000471601.2:n.6796+62_6796+63del
ENST00000359596.8:c.6796+62_6796+63del MANE Select ENSP00000352608.2:n.6796+62_6796+63del
ENST00000355481.8:c.6796+62_6796+63del ENSP00000347667.3:n.6796+62_6796+63del
ENST00000359596.7:c.6796+62_6796+63del ENSP00000352608.2:n.6796+62_6796+63del
ENST00000360985.7:c.6793+62_6793+63del ENSP00000354254.4:n.6793+62_6793+63del
ENST00000594335.5:c.248+62_248+63del
NM_000540.2:c.6796+62_6796+63del , LRG_766t1:c.6796+62_6796+63del NP_000531.2:n.6796+62_6796+63del
NM_001042723.1:c.6796+62_6796+63del NP_001036188.1:n.6796+62_6796+63del
XM_006723317.1:c.6796+62_6796+63del XP_006723380.1:n.6796+62_6796+63del
XM_006723319.1:c.6796+62_6796+63del XP_006723382.1:n.6796+62_6796+63del
XM_011527204.1:c.6793+62_6793+63del XP_011525506.1:n.6793+62_6793+63del
XM_011527205.1:c.6796+62_6796+63del XP_011525507.1:n.6796+62_6796+63del
XM_006723317.2:c.6796+62_6796+63del XP_006723380.1:n.6796+62_6796+63del
XM_006723319.2:c.6796+62_6796+63del XP_006723382.1:n.6796+62_6796+63del
XM_011527205.2:c.6796+62_6796+63del XP_011525507.1:n.6796+62_6796+63del
XR_001753735.1:n.6879+62_6879+63del
NM_000540.3:c.6796+62_6796+63del MANE Select NP_000531.2:n.6796+62_6796+63del
NM_001042723.2:c.6796+62_6796+63del NP_001036188.1:n.6796+62_6796+63del