Canonical Allele Identifier: CA2584909038
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38564895_38564905del , CM000681.2:g.38564895_38564905del GRCh38
NC_000019.9:g.39055535_39055545del , CM000681.1:g.39055535_39055545del GRCh37
NC_000019.8:g.43747375_43747385del NCBI36
NG_008866.1:g.136196_136206del , LRG_766:g.136196_136206del

Transcript Alleles

HGVS Amino-acid Change
ENST00000688602.1:c.1035-64_1035-54del
ENST00000689936.1:c.1017-64_1017-54del
ENST00000359596.8:c.12625-64_12625-54del MANE Select ENSP00000352608.2:n.12625-64_12625-54del
ENST00000355481.8:c.12610-64_12610-54del ENSP00000347667.3:n.12610-64_12610-54del
ENST00000359596.7:c.12625-64_12625-54del ENSP00000352608.2:n.12625-64_12625-54del
ENST00000360985.7:c.12607-64_12607-54del ENSP00000354254.4:n.12607-64_12607-54del
ENST00000594335.5:c.5994-64_5994-54del
NM_000540.2:c.12625-64_12625-54del , LRG_766t1:c.12625-64_12625-54del NP_000531.2:n.12625-64_12625-54del
NM_001042723.1:c.12610-64_12610-54del NP_001036188.1:n.12610-64_12610-54del
XM_006723317.1:c.12607-64_12607-54del XP_006723380.1:n.12607-64_12607-54del
XM_006723319.1:c.12592-64_12592-54del XP_006723382.1:n.12592-64_12592-54del
XM_011527204.1:c.12622-64_12622-54del XP_011525506.1:n.12622-64_12622-54del
XM_011527205.1:c.12625-64_12625-54del XP_011525507.1:n.12625-64_12625-54del
XM_006723317.2:c.12607-64_12607-54del XP_006723380.1:n.12607-64_12607-54del
XM_006723319.2:c.12592-64_12592-54del XP_006723382.1:n.12592-64_12592-54del
XM_011527205.2:c.12625-64_12625-54del XP_011525507.1:n.12625-64_12625-54del
NM_000540.3:c.12625-64_12625-54del MANE Select NP_000531.2:n.12625-64_12625-54del
NM_001042723.2:c.12610-64_12610-54del NP_001036188.1:n.12610-64_12610-54del