Canonical Allele Identifier: CA405691826

Gene: RYR1

Linked Data

• ClinVar Variation Id: 2909108
• ClinVar RCV Id: RCV003757021
• MyVariant Identifiers: chr19:g.39008065C>T (hg19) ; chr19:g.38517425C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38517425C>T , CM000681.2:g.38517425C>T	GRCh38
NC_000019.9:g.39008065C>T , CM000681.1:g.39008065C>T	GRCh37
NC_000019.8:g.43699905C>T	NCBI36
NG_008866.1:g.88726C>T , LRG_766:g.88726C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.9691C>T	ENSP00000471601.2:n.9691C>T
ENST00000359596.8:c.9752C>T MANE Select	ENSP00000352608.2:p.Ala3251Val
ENST00000355481.8:c.9752C>T	ENSP00000347667.3:p.Ala3251Val
ENST00000359596.7:c.9752C>T	ENSP00000352608.2:p.Ala3251Val
ENST00000360985.7:c.9749C>T	ENSP00000354254.4:p.Ala3250Val
ENST00000594335.5:c.3154C>T
ENST00000599547.5:c.559C>T
NM_000540.2:c.9752C>T , LRG_766t1:c.9752C>T	NP_000531.2:p.Ala3251Val
NM_001042723.1:c.9752C>T	NP_001036188.1:p.Ala3251Val
XM_006723317.1:c.9752C>T	XP_006723380.1:p.Ala3251Val
XM_006723319.1:c.9752C>T	XP_006723382.1:p.Ala3251Val
XM_011527204.1:c.9749C>T	XP_011525506.1:p.Ala3250Val
XM_011527205.1:c.9752C>T	XP_011525507.1:p.Ala3251Val
XM_006723317.2:c.9752C>T	XP_006723380.1:p.Ala3251Val
XM_006723319.2:c.9752C>T	XP_006723382.1:p.Ala3251Val
XM_011527205.2:c.9752C>T	XP_011525507.1:p.Ala3251Val
XR_001753735.1:n.9785C>T
NM_000540.3:c.9752C>T MANE Select	NP_000531.2:p.Ala3251Val
NM_001042723.2:c.9752C>T	NP_001036188.1:p.Ala3251Val