Canonical Allele Identifier: CA2335053132
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38500190_38500191delinsCT , CM000681.2:g.38500190_38500191delinsCT GRCh38
NC_000019.9:g.38990830_38990831delinsCT , CM000681.1:g.38990830_38990831delinsCT GRCh37
NC_000019.8:g.43682670_43682671delinsCT NCBI36
NG_008866.1:g.71491_71492delinsCT , LRG_766:g.71491_71492delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7323+174_7323+175delinsCT ENSP00000471601.2:n.7323+174_7323+175delinsCT
ENST00000359596.8:c.7323+174_7323+175delinsCT MANE Select ENSP00000352608.2:n.7323+174_7323+175delinsCT
ENST00000355481.8:c.7323+174_7323+175delinsCT ENSP00000347667.3:n.7323+174_7323+175delinsCT
ENST00000359596.7:c.7323+174_7323+175delinsCT ENSP00000352608.2:n.7323+174_7323+175delinsCT
ENST00000360985.7:c.7320+174_7320+175delinsCT ENSP00000354254.4:n.7320+174_7320+175delinsCT
ENST00000594335.5:c.775+174_775+175delinsCT
NM_000540.2:c.7323+174_7323+175delinsCT , LRG_766t1:c.7323+174_7323+175delinsCT NP_000531.2:n.7323+174_7323+175delinsCT
NM_001042723.1:c.7323+174_7323+175delinsCT NP_001036188.1:n.7323+174_7323+175delinsCT
XM_006723317.1:c.7323+174_7323+175delinsCT XP_006723380.1:n.7323+174_7323+175delinsCT
XM_006723319.1:c.7323+174_7323+175delinsCT XP_006723382.1:n.7323+174_7323+175delinsCT
XM_011527204.1:c.7320+174_7320+175delinsCT XP_011525506.1:n.7320+174_7320+175delinsCT
XM_011527205.1:c.7323+174_7323+175delinsCT XP_011525507.1:n.7323+174_7323+175delinsCT
XM_006723317.2:c.7323+174_7323+175delinsCT XP_006723380.1:n.7323+174_7323+175delinsCT
XM_006723319.2:c.7323+174_7323+175delinsCT XP_006723382.1:n.7323+174_7323+175delinsCT
XM_011527205.2:c.7323+174_7323+175delinsCT XP_011525507.1:n.7323+174_7323+175delinsCT
XR_001753735.1:n.7406+174_7406+175delinsCT
NM_000540.3:c.7323+174_7323+175delinsCT MANE Select NP_000531.2:n.7323+174_7323+175delinsCT
NM_001042723.2:c.7323+174_7323+175delinsCT NP_001036188.1:n.7323+174_7323+175delinsCT