Canonical Allele Identifier: CA405693508

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38517691G>A , CM000681.2:g.38517691G>A	GRCh38
NC_000019.9:g.39008331G>A , CM000681.1:g.39008331G>A	GRCh37
NC_000019.8:g.43700171G>A	NCBI36
NG_008866.1:g.88992G>A , LRG_766:g.88992G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000540.3:c.10018G>A MANE Select	NP_000531.2:p.Val3340Met
ENST00000359596.8:c.10018G>A MANE Select	ENSP00000352608.2:p.Val3340Met
NM_000540.2:c.10018G>A , LRG_766t1:c.10018G>A	NP_000531.2:p.Val3340Met
NM_001042723.1:c.10018G>A	NP_001036188.1:p.Val3340Met
NM_001042723.2:c.10018G>A	NP_001036188.1:p.Val3340Met
ENST00000355481.8:c.10018G>A	ENSP00000347667.3:p.Val3340Met
ENST00000359596.7:c.10018G>A	ENSP00000352608.2:p.Val3340Met
ENST00000360985.7:c.10015G>A	ENSP00000354254.4:p.Val3339Met
ENST00000594335.5:c.3420G>A
ENST00000599547.5:c.825G>A
ENST00000599547.6:c.9957G>A	ENSP00000471601.2:n.9957G>A
XM_006723317.1:c.10018G>A	XP_006723380.1:p.Val3340Met
XM_006723317.2:c.10018G>A	XP_006723380.1:p.Val3340Met
XM_006723319.1:c.10018G>A	XP_006723382.1:p.Val3340Met
XM_006723319.2:c.10018G>A	XP_006723382.1:p.Val3340Met
XM_011527204.1:c.10015G>A	XP_011525506.1:p.Val3339Met
XM_011527205.1:c.10018G>A	XP_011525507.1:p.Val3340Met
XM_011527205.2:c.10018G>A	XP_011525507.1:p.Val3340Met