Canonical Allele Identifier: CA915953039
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692285
ClinVar RCV Id: RCV000855476
dbSNP Id: rs1599673988

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38584928_38584945del , CM000681.2:g.38584928_38584945del GRCh38
NC_000019.9:g.39075568_39075585del , CM000681.1:g.39075568_39075585del GRCh37
NC_000019.8:g.43767408_43767425del NCBI36
NG_008866.1:g.156229_156246del , LRG_766:g.156229_156246del

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.1583-15_1585del
ENST00000688602.1:c.2980-15_2982del
ENST00000689936.1:c.2952-15_2954del
ENST00000692547.1:n.25_42del
ENST00000359596.8:c.14647-15_14649del
ENST00000355481.8:c.14632-15_14634del
ENST00000359596.7:c.14647-15_14649del
ENST00000360985.7:c.14629-15_14631del
NM_000540.2:c.14647-15_14649del , LRG_766t1:c.14647-15_14649del
NM_001042723.1:c.14632-15_14634del
XM_006723317.1:c.14629-15_14631del
XM_006723319.1:c.14614-15_14616del
XM_011527204.1:c.14644-15_14646del
XM_011527205.1:c.14560-15_14562del
XM_006723317.2:c.14629-15_14631del
XM_006723319.2:c.14614-15_14616del
XM_011527205.2:c.14560-15_14562del
NM_000540.3:c.14647-15_14649del
NM_001042723.2:c.14632-15_14634del