Canonical Allele Identifier: CA2843407553

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543898T>A , CM000681.2:g.38543898T>A	GRCh38
NC_000019.9:g.39034538T>A , CM000681.1:g.39034538T>A	GRCh37
NC_000019.8:g.43726378T>A	NCBI36
NG_008866.1:g.115199T>A , LRG_766:g.115199T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.422+23T>A
ENST00000689936.1:c.404+23T>A
ENST00000359596.8:c.12012+23T>A MANE Select	ENSP00000352608.2:n.12012+23T>A
ENST00000355481.8:c.11997+23T>A	ENSP00000347667.3:n.11997+23T>A
ENST00000359596.7:c.12012+23T>A	ENSP00000352608.2:n.12012+23T>A
ENST00000360985.7:c.11994+23T>A	ENSP00000354254.4:n.11994+23T>A
ENST00000593322.1:c.621+23T>A
ENST00000594335.5:c.5381+23T>A
NM_000540.2:c.12012+23T>A , LRG_766t1:c.12012+23T>A	NP_000531.2:n.12012+23T>A
NM_001042723.1:c.11997+23T>A	NP_001036188.1:n.11997+23T>A
XM_006723317.1:c.11994+23T>A	XP_006723380.1:n.11994+23T>A
XM_006723319.1:c.11979+23T>A	XP_006723382.1:n.11979+23T>A
XM_011527204.1:c.12009+23T>A	XP_011525506.1:n.12009+23T>A
XM_011527205.1:c.12012+23T>A	XP_011525507.1:n.12012+23T>A
XM_006723317.2:c.11994+23T>A	XP_006723380.1:n.11994+23T>A
XM_006723319.2:c.11979+23T>A	XP_006723382.1:n.11979+23T>A
XM_011527205.2:c.12012+23T>A	XP_011525507.1:n.12012+23T>A
NM_000540.3:c.12012+23T>A MANE Select	NP_000531.2:n.12012+23T>A
NM_001042723.2:c.11997+23T>A	NP_001036188.1:n.11997+23T>A