Canonical Allele Identifier: CA2736066229
Gene: RYR1 HGNC NCBI

Linked Data

dbSNP Id: rs2145911049

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38584564_38584598del , CM000681.2:g.38584564_38584598del GRCh38
NC_000019.9:g.39075204_39075238del , CM000681.1:g.39075204_39075238del GRCh37
NC_000019.8:g.43767044_43767078del NCBI36
NG_008866.1:g.155865_155899del , LRG_766:g.155865_155899del

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1583-379_1583-345del
ENST00000688602.1:c.2980-379_2980-345del
ENST00000689936.1:c.2952-379_2952-345del
ENST00000359596.8:c.14647-379_14647-345del MANE Select ENSP00000352608.2:n.14647-379_14647-345del
ENST00000355481.8:c.14632-379_14632-345del ENSP00000347667.3:n.14632-379_14632-345del
ENST00000359596.7:c.14647-379_14647-345del ENSP00000352608.2:n.14647-379_14647-345del
ENST00000360985.7:c.14629-379_14629-345del ENSP00000354254.4:n.14629-379_14629-345del
NM_000540.2:c.14647-379_14647-345del , LRG_766t1:c.14647-379_14647-345del NP_000531.2:n.14647-379_14647-345del
NM_001042723.1:c.14632-379_14632-345del NP_001036188.1:n.14632-379_14632-345del
XM_006723317.1:c.14629-379_14629-345del XP_006723380.1:n.14629-379_14629-345del
XM_006723319.1:c.14614-379_14614-345del XP_006723382.1:n.14614-379_14614-345del
XM_011527204.1:c.14644-379_14644-345del XP_011525506.1:n.14644-379_14644-345del
XM_011527205.1:c.14560-379_14560-345del XP_011525507.1:n.14560-379_14560-345del
XM_006723317.2:c.14629-379_14629-345del XP_006723380.1:n.14629-379_14629-345del
XM_006723319.2:c.14614-379_14614-345del XP_006723382.1:n.14614-379_14614-345del
XM_011527205.2:c.14560-379_14560-345del XP_011525507.1:n.14560-379_14560-345del
NM_000540.3:c.14647-379_14647-345del MANE Select NP_000531.2:n.14647-379_14647-345del
NM_001042723.2:c.14632-379_14632-345del NP_001036188.1:n.14632-379_14632-345del