Canonical Allele Identifier: CA071346

Gene: RYR1

Linked Data

• ClinVar Variation Id: 3070653
• ClinVar RCV Id: RCV004013163
• dbSNP Id: rs772107322
• ExAC: 19:38994996 A / G
• gnomAD v2: 19-38994996-A-G
• gnomAD v4: 19-38504356-A-G
• MyVariant Identifiers: chr19:g.38994996A>G (hg19) ; chr19:g.38504356A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38504356A>G , CM000681.2:g.38504356A>G	GRCh38
NC_000019.9:g.38994996A>G , CM000681.1:g.38994996A>G	GRCh37
NC_000019.8:g.43686836A>G	NCBI36
NG_008866.1:g.75657A>G , LRG_766:g.75657A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.8063A>G	ENSP00000471601.2:p.His2688Arg
ENST00000359596.8:c.8063A>G MANE Select	ENSP00000352608.2:p.His2688Arg
ENST00000355481.8:c.8063A>G	ENSP00000347667.3:p.His2688Arg
ENST00000359596.7:c.8063A>G	ENSP00000352608.2:p.His2688Arg
ENST00000360985.7:c.8060A>G	ENSP00000354254.4:p.His2687Arg
ENST00000594335.5:c.1515A>G
NM_000540.2:c.8063A>G , LRG_766t1:c.8063A>G	NP_000531.2:p.His2688Arg
NM_001042723.1:c.8063A>G	NP_001036188.1:p.His2688Arg
XM_006723317.1:c.8063A>G	XP_006723380.1:p.His2688Arg
XM_006723319.1:c.8063A>G	XP_006723382.1:p.His2688Arg
XM_011527204.1:c.8060A>G	XP_011525506.1:p.His2687Arg
XM_011527205.1:c.8063A>G	XP_011525507.1:p.His2688Arg
XM_006723317.2:c.8063A>G	XP_006723380.1:p.His2688Arg
XM_006723319.2:c.8063A>G	XP_006723382.1:p.His2688Arg
XM_011527205.2:c.8063A>G	XP_011525507.1:p.His2688Arg
XR_001753735.1:n.8146A>G
NM_000540.3:c.8063A>G MANE Select	NP_000531.2:p.His2688Arg
NM_001042723.2:c.8063A>G	NP_001036188.1:p.His2688Arg