Canonical Allele Identifier: CA060694

Gene: RYR1

Linked Data

• dbSNP Id: rs770800347
• ExAC: 19:39062936 GC / G
• gnomAD v2: 19-39062936-GC-G
• MyVariant Identifiers: chr19:g.39062937del (hg19) ; chr19:g.38572297del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38572297del , CM000681.2:g.38572297del	GRCh38
NC_000019.9:g.39062937del , CM000681.1:g.39062937del	GRCh37
NC_000019.8:g.43754777del	NCBI36
NG_008866.1:g.143598del , LRG_766:g.143598del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.934+27del
ENST00000688602.1:c.2331+27del
ENST00000689936.1:c.2303+27del
ENST00000359596.8:c.13998+27del MANE Select	ENSP00000352608.2:n.13998+27del
ENST00000355481.8:c.13983+27del	ENSP00000347667.3:n.13983+27del
ENST00000359596.7:c.13998+27del	ENSP00000352608.2:n.13998+27del
ENST00000360985.7:c.13980+27del	ENSP00000354254.4:n.13980+27del
NM_000540.2:c.13998+27del , LRG_766t1:c.13998+27del	NP_000531.2:n.13998+27del
NM_001042723.1:c.13983+27del	NP_001036188.1:n.13983+27del
XM_006723317.1:c.13980+27del	XP_006723380.1:n.13980+27del
XM_006723319.1:c.13965+27del	XP_006723382.1:n.13965+27del
XM_011527204.1:c.13995+27del	XP_011525506.1:n.13995+27del
XM_011527205.1:c.13911+27del	XP_011525507.1:n.13911+27del
XM_006723317.2:c.13980+27del	XP_006723380.1:n.13980+27del
XM_006723319.2:c.13965+27del	XP_006723382.1:n.13965+27del
XM_011527205.2:c.13911+27del	XP_011525507.1:n.13911+27del
NM_000540.3:c.13998+27del MANE Select	NP_000531.2:n.13998+27del
NM_001042723.2:c.13983+27del	NP_001036188.1:n.13983+27del