Canonical Allele Identifier: CA2335046110
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38485549_38485553delinsCTCAT , CM000681.2:g.38485549_38485553delinsCTCAT GRCh38
NC_000019.9:g.38976189_38976193delinsCTCAT , CM000681.1:g.38976189_38976193delinsCTCAT GRCh37
NC_000019.8:g.43668029_43668033delinsCTCAT NCBI36
NG_008866.1:g.56850_56854delinsCTCAT , LRG_766:g.56850_56854delinsCTCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.4935-41_4935-37delinsCTCAT ENSP00000471601.2:n.4935-41_4935-37delinsCTCAT
ENST00000359596.8:c.4935-41_4935-37delinsCTCAT MANE Select ENSP00000352608.2:n.4935-41_4935-37delinsCTCAT
ENST00000355481.8:c.4935-41_4935-37delinsCTCAT ENSP00000347667.3:n.4935-41_4935-37delinsCTCAT
ENST00000359596.7:c.4935-41_4935-37delinsCTCAT ENSP00000352608.2:n.4935-41_4935-37delinsCTCAT
ENST00000360985.7:c.4932-41_4932-37delinsCTCAT ENSP00000354254.4:n.4932-41_4932-37delinsCTCAT
NM_000540.2:c.4935-41_4935-37delinsCTCAT , LRG_766t1:c.4935-41_4935-37delinsCTCAT NP_000531.2:n.4935-41_4935-37delinsCTCAT
NM_001042723.1:c.4935-41_4935-37delinsCTCAT NP_001036188.1:n.4935-41_4935-37delinsCTCAT
XM_006723317.1:c.4935-41_4935-37delinsCTCAT XP_006723380.1:n.4935-41_4935-37delinsCTCAT
XM_006723319.1:c.4935-41_4935-37delinsCTCAT XP_006723382.1:n.4935-41_4935-37delinsCTCAT
XM_011527204.1:c.4932-41_4932-37delinsCTCAT XP_011525506.1:n.4932-41_4932-37delinsCTCAT
XM_011527205.1:c.4935-41_4935-37delinsCTCAT XP_011525507.1:n.4935-41_4935-37delinsCTCAT
XM_006723317.2:c.4935-41_4935-37delinsCTCAT XP_006723380.1:n.4935-41_4935-37delinsCTCAT
XM_006723319.2:c.4935-41_4935-37delinsCTCAT XP_006723382.1:n.4935-41_4935-37delinsCTCAT
XM_011527205.2:c.4935-41_4935-37delinsCTCAT XP_011525507.1:n.4935-41_4935-37delinsCTCAT
XR_001753735.1:n.5018-41_5018-37delinsCTCAT
NM_000540.3:c.4935-41_4935-37delinsCTCAT MANE Select NP_000531.2:n.4935-41_4935-37delinsCTCAT
NM_001042723.2:c.4935-41_4935-37delinsCTCAT NP_001036188.1:n.4935-41_4935-37delinsCTCAT