Canonical Allele Identifier: CA405691230

Gene: RYR1

Linked Data

• ClinVar Variation Id: 3075002
• ClinVar RCV Id: RCV004015528
• MyVariant Identifiers: chr19:g.38946317G>A (hg19) ; chr19:g.38455677G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38455677G>A , CM000681.2:g.38455677G>A	GRCh38
NC_000019.9:g.38946317G>A , CM000681.1:g.38946317G>A	GRCh37
NC_000019.8:g.43638157G>A	NCBI36
NG_008866.1:g.26978G>A , LRG_766:g.26978G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.1717G>A	ENSP00000471601.2:p.Val573Ile
ENST00000359596.8:c.1717G>A MANE Select	ENSP00000352608.2:p.Val573Ile
ENST00000355481.8:c.1717G>A	ENSP00000347667.3:p.Val573Ile
ENST00000359596.7:c.1717G>A	ENSP00000352608.2:p.Val573Ile
ENST00000360985.7:c.1717G>A	ENSP00000354254.4:p.Val573Ile
NM_000540.2:c.1717G>A , LRG_766t1:c.1717G>A	NP_000531.2:p.Val573Ile
NM_001042723.1:c.1717G>A	NP_001036188.1:p.Val573Ile
XM_006723317.1:c.1717G>A	XP_006723380.1:p.Val573Ile
XM_006723319.1:c.1717G>A	XP_006723382.1:p.Val573Ile
XM_011527204.1:c.1714G>A	XP_011525506.1:p.Val572Ile
XM_011527205.1:c.1717G>A	XP_011525507.1:p.Val573Ile
XM_006723317.2:c.1717G>A	XP_006723380.1:p.Val573Ile
XM_006723319.2:c.1717G>A	XP_006723382.1:p.Val573Ile
XM_011527205.2:c.1717G>A	XP_011525507.1:p.Val573Ile
XR_001753735.1:n.1800G>A
NM_000540.3:c.1717G>A MANE Select	NP_000531.2:p.Val573Ile
NM_001042723.2:c.1717G>A	NP_001036188.1:p.Val573Ile