Canonical Allele Identifier: CA308123001

Gene: RYR1

Linked Data

• ClinVar Variation Id: 3069511
• ClinVar RCV Id: RCV004008055
• dbSNP Id: rs1030637532
• gnomAD v4: 19-38455316-G-C
• MyVariant Identifiers: chr19:g.38945956G>C (hg19) ; chr19:g.38455316G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38455316G>C , CM000681.2:g.38455316G>C	GRCh38
NC_000019.9:g.38945956G>C , CM000681.1:g.38945956G>C	GRCh37
NC_000019.8:g.43637796G>C	NCBI36
NG_008866.1:g.26617G>C , LRG_766:g.26617G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.1522G>C	ENSP00000471601.2:p.Glu508Gln
ENST00000359596.8:c.1522G>C MANE Select	ENSP00000352608.2:p.Glu508Gln
ENST00000355481.8:c.1522G>C	ENSP00000347667.3:p.Glu508Gln
ENST00000359596.7:c.1522G>C	ENSP00000352608.2:p.Glu508Gln
ENST00000360985.7:c.1522G>C	ENSP00000354254.4:p.Glu508Gln
NM_000540.2:c.1522G>C , LRG_766t1:c.1522G>C	NP_000531.2:p.Glu508Gln
NM_001042723.1:c.1522G>C	NP_001036188.1:p.Glu508Gln
XM_006723317.1:c.1522G>C	XP_006723380.1:p.Glu508Gln
XM_006723319.1:c.1522G>C	XP_006723382.1:p.Glu508Gln
XM_011527204.1:c.1519G>C	XP_011525506.1:p.Glu507Gln
XM_011527205.1:c.1522G>C	XP_011525507.1:p.Glu508Gln
XM_006723317.2:c.1522G>C	XP_006723380.1:p.Glu508Gln
XM_006723319.2:c.1522G>C	XP_006723382.1:p.Glu508Gln
XM_011527205.2:c.1522G>C	XP_011525507.1:p.Glu508Gln
XR_001753735.1:n.1605G>C
NM_000540.3:c.1522G>C MANE Select	NP_000531.2:p.Glu508Gln
NM_001042723.2:c.1522G>C	NP_001036188.1:p.Glu508Gln