Canonical Allele Identifier: CA2739276753

Gene: RYR1

Linked Data

• ClinVar Variation Id: 2829142
• ClinVar RCV Id: RCV003757574

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543882_38543891del , CM000681.2:g.38543882_38543891del	GRCh38
NC_000019.9:g.39034522_39034531del , CM000681.1:g.39034522_39034531del	GRCh37
NC_000019.8:g.43726362_43726371del	NCBI36
NG_008866.1:g.115183_115192del , LRG_766:g.115183_115192del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.422+7_422+16del
ENST00000689936.1:c.404+7_404+16del
ENST00000359596.8:c.12012+7_12012+16del MANE Select	ENSP00000352608.2:n.12012+7_12012+16del
ENST00000355481.8:c.11997+7_11997+16del	ENSP00000347667.3:n.11997+7_11997+16del
ENST00000359596.7:c.12012+7_12012+16del	ENSP00000352608.2:n.12012+7_12012+16del
ENST00000360985.7:c.11994+7_11994+16del	ENSP00000354254.4:n.11994+7_11994+16del
ENST00000593322.1:c.621+7_621+16del
ENST00000594335.5:c.5381+7_5381+16del
NM_000540.2:c.12012+7_12012+16del , LRG_766t1:c.12012+7_12012+16del	NP_000531.2:n.12012+7_12012+16del
NM_001042723.1:c.11997+7_11997+16del	NP_001036188.1:n.11997+7_11997+16del
XM_006723317.1:c.11994+7_11994+16del	XP_006723380.1:n.11994+7_11994+16del
XM_006723319.1:c.11979+7_11979+16del	XP_006723382.1:n.11979+7_11979+16del
XM_011527204.1:c.12009+7_12009+16del	XP_011525506.1:n.12009+7_12009+16del
XM_011527205.1:c.12012+7_12012+16del	XP_011525507.1:n.12012+7_12012+16del
XM_006723317.2:c.11994+7_11994+16del	XP_006723380.1:n.11994+7_11994+16del
XM_006723319.2:c.11979+7_11979+16del	XP_006723382.1:n.11979+7_11979+16del
XM_011527205.2:c.12012+7_12012+16del	XP_011525507.1:n.12012+7_12012+16del
NM_000540.3:c.12012+7_12012+16del MANE Select	NP_000531.2:n.12012+7_12012+16del
NM_001042723.2:c.11997+7_11997+16del	NP_001036188.1:n.11997+7_11997+16del