Canonical Allele Identifier: CA2843139614

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38573357_38573360del , CM000681.2:g.38573357_38573360del	GRCh38
NC_000019.9:g.39063997_39064000del , CM000681.1:g.39063997_39064000del	GRCh37
NC_000019.8:g.43755837_43755840del	NCBI36
NG_008866.1:g.144658_144661del , LRG_766:g.144658_144661del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1065+50_1065+53del
ENST00000688602.1:c.2462+50_2462+53del
ENST00000689936.1:c.2434+50_2434+53del
ENST00000359596.8:c.14129+50_14129+53del MANE Select	ENSP00000352608.2:n.14129+50_14129+53del
ENST00000355481.8:c.14114+50_14114+53del	ENSP00000347667.3:n.14114+50_14114+53del
ENST00000359596.7:c.14129+50_14129+53del	ENSP00000352608.2:n.14129+50_14129+53del
ENST00000360985.7:c.14111+50_14111+53del	ENSP00000354254.4:n.14111+50_14111+53del
NM_000540.2:c.14129+50_14129+53del , LRG_766t1:c.14129+50_14129+53del	NP_000531.2:n.14129+50_14129+53del
NM_001042723.1:c.14114+50_14114+53del	NP_001036188.1:n.14114+50_14114+53del
XM_006723317.1:c.14111+50_14111+53del	XP_006723380.1:n.14111+50_14111+53del
XM_006723319.1:c.14096+50_14096+53del	XP_006723382.1:n.14096+50_14096+53del
XM_011527204.1:c.14126+50_14126+53del	XP_011525506.1:n.14126+50_14126+53del
XM_011527205.1:c.14042+50_14042+53del	XP_011525507.1:n.14042+50_14042+53del
XM_006723317.2:c.14111+50_14111+53del	XP_006723380.1:n.14111+50_14111+53del
XM_006723319.2:c.14096+50_14096+53del	XP_006723382.1:n.14096+50_14096+53del
XM_011527205.2:c.14042+50_14042+53del	XP_011525507.1:n.14042+50_14042+53del
NM_000540.3:c.14129+50_14129+53del MANE Select	NP_000531.2:n.14129+50_14129+53del
NM_001042723.2:c.14114+50_14114+53del	NP_001036188.1:n.14114+50_14114+53del