Canonical Allele Identifier: CA2580096942

Gene: RYR1

Linked Data

• ClinVar Variation Id: 2030989
• ClinVar RCV Id: RCV002872115

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38457485C>T , CM000681.2:g.38457485C>T	GRCh38
NC_000019.9:g.38948125C>T , CM000681.1:g.38948125C>T	GRCh37
NC_000019.8:g.43639965C>T	NCBI36
NG_008866.1:g.28786C>T , LRG_766:g.28786C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000599547.6:c.1792-12C>T	ENSP00000471601.2:n.1792-12C>T
ENST00000359596.8:c.1792-12C>T MANE Select	ENSP00000352608.2:n.1792-12C>T
ENST00000355481.8:c.1792-12C>T	ENSP00000347667.3:n.1792-12C>T
ENST00000359596.7:c.1792-12C>T	ENSP00000352608.2:n.1792-12C>T
ENST00000360985.7:c.1792-12C>T	ENSP00000354254.4:n.1792-12C>T
NM_000540.2:c.1792-12C>T , LRG_766t1:c.1792-12C>T	NP_000531.2:n.1792-12C>T
NM_001042723.1:c.1792-12C>T	NP_001036188.1:n.1792-12C>T
XM_006723317.1:c.1792-12C>T	XP_006723380.1:n.1792-12C>T
XM_006723319.1:c.1792-12C>T	XP_006723382.1:n.1792-12C>T
XM_011527204.1:c.1789-12C>T	XP_011525506.1:n.1789-12C>T
XM_011527205.1:c.1792-12C>T	XP_011525507.1:n.1792-12C>T
XM_006723317.2:c.1792-12C>T	XP_006723380.1:n.1792-12C>T
XM_006723319.2:c.1792-12C>T	XP_006723382.1:n.1792-12C>T
XM_011527205.2:c.1792-12C>T	XP_011525507.1:n.1792-12C>T
XR_001753735.1:n.1875-12C>T
NM_000540.3:c.1792-12C>T MANE Select	NP_000531.2:n.1792-12C>T
NM_001042723.2:c.1792-12C>T	NP_001036188.1:n.1792-12C>T