Canonical Allele Identifier: CA405691878

Gene: RYR1

Linked Data

• ClinVar Variation Id: 3070906
• ClinVar RCV Id: RCV004014408
• MyVariant Identifiers: chr19:g.39008074G>T (hg19) ; chr19:g.38517434G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38517434G>T , CM000681.2:g.38517434G>T	GRCh38
NC_000019.9:g.39008074G>T , CM000681.1:g.39008074G>T	GRCh37
NC_000019.8:g.43699914G>T	NCBI36
NG_008866.1:g.88735G>T , LRG_766:g.88735G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.9700G>T	ENSP00000471601.2:n.9700G>T
ENST00000359596.8:c.9761G>T MANE Select	ENSP00000352608.2:p.Gly3254Val
ENST00000355481.8:c.9761G>T	ENSP00000347667.3:p.Gly3254Val
ENST00000359596.7:c.9761G>T	ENSP00000352608.2:p.Gly3254Val
ENST00000360985.7:c.9758G>T	ENSP00000354254.4:p.Gly3253Val
ENST00000594335.5:c.3163G>T
ENST00000599547.5:c.568G>T
NM_000540.2:c.9761G>T , LRG_766t1:c.9761G>T	NP_000531.2:p.Gly3254Val
NM_001042723.1:c.9761G>T	NP_001036188.1:p.Gly3254Val
XM_006723317.1:c.9761G>T	XP_006723380.1:p.Gly3254Val
XM_006723319.1:c.9761G>T	XP_006723382.1:p.Gly3254Val
XM_011527204.1:c.9758G>T	XP_011525506.1:p.Gly3253Val
XM_011527205.1:c.9761G>T	XP_011525507.1:p.Gly3254Val
XM_006723317.2:c.9761G>T	XP_006723380.1:p.Gly3254Val
XM_006723319.2:c.9761G>T	XP_006723382.1:p.Gly3254Val
XM_011527205.2:c.9761G>T	XP_011525507.1:p.Gly3254Val
NM_000540.3:c.9761G>T MANE Select	NP_000531.2:p.Gly3254Val
NM_001042723.2:c.9761G>T	NP_001036188.1:p.Gly3254Val