Canonical Allele Identifier: CA056930

Gene: RYR1

Linked Data

• ClinVar Variation Id: 256404
• ClinVar RCV Id: RCV000246426 ; RCV000279931 ; RCV000351142 ; RCV000312561 ; RCV000392603 ; RCV001087535
• dbSNP Id: rs369650355
• ExAC: 19:39025869 G / A
• gnomAD v2: 19-39025869-G-A
• gnomAD v3: 19-38535229-G-A
• gnomAD v4: 19-38535229-G-A
• MyVariant Identifiers: chr19:g.39025869G>A (hg19) ; chr19:g.38535229G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38535229G>A , CM000681.2:g.38535229G>A	GRCh38
NC_000019.9:g.39025869G>A , CM000681.1:g.39025869G>A	GRCh37
NC_000019.8:g.43717709G>A	NCBI36
NG_008866.1:g.106530G>A , LRG_766:g.106530G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.11378+9G>A	ENSP00000471601.2:n.11378+9G>A
ENST00000359596.8:c.11439+9G>A MANE Select	ENSP00000352608.2:n.11439+9G>A
ENST00000355481.8:c.11424+9G>A	ENSP00000347667.3:n.11424+9G>A
ENST00000359596.7:c.11439+9G>A	ENSP00000352608.2:n.11439+9G>A
ENST00000360985.7:c.11421+9G>A	ENSP00000354254.4:n.11421+9G>A
ENST00000593322.1:c.140+9G>A
ENST00000594335.5:c.4826+9G>A
ENST00000596431.5:c.168+9G>A	ENSP00000470848.1:n.168+9G>A
ENST00000601514.5:c.720+9G>A	ENSP00000472497.1:n.720+9G>A
NM_000540.2:c.11439+9G>A , LRG_766t1:c.11439+9G>A	NP_000531.2:n.11439+9G>A
NM_001042723.1:c.11424+9G>A	NP_001036188.1:n.11424+9G>A
XM_006723317.1:c.11439+9G>A	XP_006723380.1:n.11439+9G>A
XM_006723319.1:c.11424+9G>A	XP_006723382.1:n.11424+9G>A
XM_011527204.1:c.11436+9G>A	XP_011525506.1:n.11436+9G>A
XM_011527205.1:c.11439+9G>A	XP_011525507.1:n.11439+9G>A
XM_006723317.2:c.11439+9G>A	XP_006723380.1:n.11439+9G>A
XM_006723319.2:c.11424+9G>A	XP_006723382.1:n.11424+9G>A
XM_011527205.2:c.11439+9G>A	XP_011525507.1:n.11439+9G>A
NM_000540.3:c.11439+9G>A MANE Select	NP_000531.2:n.11439+9G>A
NM_001042723.2:c.11424+9G>A	NP_001036188.1:n.11424+9G>A