Canonical Allele Identifier: CA10651890

Gene: RYR1

Linked Data

• ClinVar Variation Id: 329111
• ClinVar RCV Id: RCV000302219 ; RCV000359696 ; RCV000360509 ; RCV000408133 ; RCV003757172
• dbSNP Id: rs886054402
• MyVariant Identifiers: chr19:g.39034308G>A (hg19) ; chr19:g.38543668G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543668G>A , CM000681.2:g.38543668G>A	GRCh38
NC_000019.9:g.39034308G>A , CM000681.1:g.39034308G>A	GRCh37
NC_000019.8:g.43726148G>A	NCBI36
NG_008866.1:g.114969G>A , LRG_766:g.114969G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.317+8G>A
ENST00000689936.1:c.299+8G>A
ENST00000359596.8:c.11907+8G>A MANE Select	ENSP00000352608.2:n.11907+8G>A
ENST00000355481.8:c.11892+8G>A	ENSP00000347667.3:n.11892+8G>A
ENST00000359596.7:c.11907+8G>A	ENSP00000352608.2:n.11907+8G>A
ENST00000360985.7:c.11889+8G>A	ENSP00000354254.4:n.11889+8G>A
ENST00000593322.1:c.516+8G>A
ENST00000594335.5:c.5276+8G>A
NM_000540.2:c.11907+8G>A , LRG_766t1:c.11907+8G>A	NP_000531.2:n.11907+8G>A
NM_001042723.1:c.11892+8G>A	NP_001036188.1:n.11892+8G>A
XM_006723317.1:c.11889+8G>A	XP_006723380.1:n.11889+8G>A
XM_006723319.1:c.11874+8G>A	XP_006723382.1:n.11874+8G>A
XM_011527204.1:c.11904+8G>A	XP_011525506.1:n.11904+8G>A
XM_011527205.1:c.11907+8G>A	XP_011525507.1:n.11907+8G>A
XM_006723317.2:c.11889+8G>A	XP_006723380.1:n.11889+8G>A
XM_006723319.2:c.11874+8G>A	XP_006723382.1:n.11874+8G>A
XM_011527205.2:c.11907+8G>A	XP_011525507.1:n.11907+8G>A
NM_000540.3:c.11907+8G>A MANE Select	NP_000531.2:n.11907+8G>A
NM_001042723.2:c.11892+8G>A	NP_001036188.1:n.11892+8G>A