Canonical Allele Identifier: CA2814346314
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38565559_38565570del , CM000681.2:g.38565559_38565570del GRCh38
NC_000019.9:g.39056199_39056210del , CM000681.1:g.39056199_39056210del GRCh37
NC_000019.8:g.43748039_43748050del NCBI36
NG_008866.1:g.136860_136871del , LRG_766:g.136860_136871del

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.161_172del
ENST00000688602.1:c.1635_1646del
ENST00000689936.1:c.1617_1628del
ENST00000359596.8:c.13225_13236del MANE Select ENSP00000352608.2:p.Ser4409_Ala4412del
ENST00000355481.8:c.13210_13221del ENSP00000347667.3:p.Ser4404_Ala4407del
ENST00000359596.7:c.13225_13236del ENSP00000352608.2:p.Ser4409_Ala4412del
ENST00000360985.7:c.13207_13218del ENSP00000354254.4:p.Ser4403_Ala4406del
NM_000540.2:c.13225_13236del , LRG_766t1:c.13225_13236del NP_000531.2:p.Ser4409_Ala4412del
NM_001042723.1:c.13210_13221del NP_001036188.1:p.Ser4404_Ala4407del
XM_006723317.1:c.13207_13218del XP_006723380.1:p.Ser4403_Ala4406del
XM_006723319.1:c.13192_13203del XP_006723382.1:p.Ser4398_Ala4401del
XM_011527204.1:c.13222_13233del XP_011525506.1:p.Ser4408_Ala4411del
XM_011527205.1:c.13225_13236del XP_011525507.1:p.Ser4409_Ala4412del
XM_006723317.2:c.13207_13218del XP_006723380.1:p.Ser4403_Ala4406del
XM_006723319.2:c.13192_13203del XP_006723382.1:p.Ser4398_Ala4401del
XM_011527205.2:c.13225_13236del XP_011525507.1:p.Ser4409_Ala4412del
NM_000540.3:c.13225_13236del MANE Select NP_000531.2:p.Ser4409_Ala4412del
NM_001042723.2:c.13210_13221del NP_001036188.1:p.Ser4404_Ala4407del