Canonical Allele Identifier: CA2335091517
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38578439_38578440delinsTC , CM000681.2:g.38578439_38578440delinsTC GRCh38
NC_000019.9:g.39069079_39069080delinsTC , CM000681.1:g.39069079_39069080delinsTC GRCh37
NC_000019.8:g.43760919_43760920delinsTC NCBI36
NG_008866.1:g.149740_149741delinsTC , LRG_766:g.149740_149741delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1300+235_1300+236delinsTC
ENST00000688602.1:c.2697+235_2697+236delinsTC
ENST00000689936.1:c.2669+235_2669+236delinsTC
ENST00000359596.8:c.14364+235_14364+236delinsTC MANE Select ENSP00000352608.2:n.14364+235_14364+236delinsTC
ENST00000355481.8:c.14349+235_14349+236delinsTC ENSP00000347667.3:n.14349+235_14349+236delinsTC
ENST00000359596.7:c.14364+235_14364+236delinsTC ENSP00000352608.2:n.14364+235_14364+236delinsTC
ENST00000360985.7:c.14346+235_14346+236delinsTC ENSP00000354254.4:n.14346+235_14346+236delinsTC
NM_000540.2:c.14364+235_14364+236delinsTC , LRG_766t1:c.14364+235_14364+236delinsTC NP_000531.2:n.14364+235_14364+236delinsTC
NM_001042723.1:c.14349+235_14349+236delinsTC NP_001036188.1:n.14349+235_14349+236delinsTC
XM_006723317.1:c.14346+235_14346+236delinsTC XP_006723380.1:n.14346+235_14346+236delinsTC
XM_006723319.1:c.14331+235_14331+236delinsTC XP_006723382.1:n.14331+235_14331+236delinsTC
XM_011527204.1:c.14361+235_14361+236delinsTC XP_011525506.1:n.14361+235_14361+236delinsTC
XM_011527205.1:c.14277+235_14277+236delinsTC XP_011525507.1:n.14277+235_14277+236delinsTC
XM_006723317.2:c.14346+235_14346+236delinsTC XP_006723380.1:n.14346+235_14346+236delinsTC
XM_006723319.2:c.14331+235_14331+236delinsTC XP_006723382.1:n.14331+235_14331+236delinsTC
XM_011527205.2:c.14277+235_14277+236delinsTC XP_011525507.1:n.14277+235_14277+236delinsTC
NM_000540.3:c.14364+235_14364+236delinsTC MANE Select NP_000531.2:n.14364+235_14364+236delinsTC
NM_001042723.2:c.14349+235_14349+236delinsTC NP_001036188.1:n.14349+235_14349+236delinsTC