Canonical Allele Identifier: CA2335089085
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38573419_38573427delinsCACCTGTAA , CM000681.2:g.38573419_38573427delinsCACCTGTAA GRCh38
NC_000019.9:g.39064059_39064067delinsCACCTGTAA , CM000681.1:g.39064059_39064067delinsCACCTGTAA GRCh37
NC_000019.8:g.43755899_43755907delinsCACCTGTAA NCBI36
NG_008866.1:g.144720_144728delinsCACCTGTAA , LRG_766:g.144720_144728delinsCACCTGTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1065+112_1065+120delinsCACCTGTAA
ENST00000688602.1:c.2462+112_2462+120delinsCACCTGTAA
ENST00000689936.1:c.2434+112_2434+120delinsCACCTGTAA
ENST00000359596.8:c.14129+112_14129+120delinsCACCTGTAA MANE Select ENSP00000352608.2:n.14129+112_14129+120delinsCACCTGTAA
ENST00000355481.8:c.14114+112_14114+120delinsCACCTGTAA ENSP00000347667.3:n.14114+112_14114+120delinsCACCTGTAA
ENST00000359596.7:c.14129+112_14129+120delinsCACCTGTAA ENSP00000352608.2:n.14129+112_14129+120delinsCACCTGTAA
ENST00000360985.7:c.14111+112_14111+120delinsCACCTGTAA ENSP00000354254.4:n.14111+112_14111+120delinsCACCTGTAA
NM_000540.2:c.14129+112_14129+120delinsCACCTGTAA , LRG_766t1:c.14129+112_14129+120delinsCACCTGTAA NP_000531.2:n.14129+112_14129+120delinsCACCTGTAA
NM_001042723.1:c.14114+112_14114+120delinsCACCTGTAA NP_001036188.1:n.14114+112_14114+120delinsCACCTGTAA
XM_006723317.1:c.14111+112_14111+120delinsCACCTGTAA XP_006723380.1:n.14111+112_14111+120delinsCACCTGTAA
XM_006723319.1:c.14096+112_14096+120delinsCACCTGTAA XP_006723382.1:n.14096+112_14096+120delinsCACCTGTAA
XM_011527204.1:c.14126+112_14126+120delinsCACCTGTAA XP_011525506.1:n.14126+112_14126+120delinsCACCTGTAA
XM_011527205.1:c.14042+112_14042+120delinsCACCTGTAA XP_011525507.1:n.14042+112_14042+120delinsCACCTGTAA
XM_006723317.2:c.14111+112_14111+120delinsCACCTGTAA XP_006723380.1:n.14111+112_14111+120delinsCACCTGTAA
XM_006723319.2:c.14096+112_14096+120delinsCACCTGTAA XP_006723382.1:n.14096+112_14096+120delinsCACCTGTAA
XM_011527205.2:c.14042+112_14042+120delinsCACCTGTAA XP_011525507.1:n.14042+112_14042+120delinsCACCTGTAA
NM_000540.3:c.14129+112_14129+120delinsCACCTGTAA MANE Select NP_000531.2:n.14129+112_14129+120delinsCACCTGTAA
NM_001042723.2:c.14114+112_14114+120delinsCACCTGTAA NP_001036188.1:n.14114+112_14114+120delinsCACCTGTAA