Canonical Allele Identifier: CA2576827527

Gene: RYR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580513del , CM000681.2:g.38580513del	GRCh38
NC_000019.9:g.39071153del , CM000681.1:g.39071153del	GRCh37
NC_000019.8:g.43762993del	NCBI36
NG_008866.1:g.151814del , LRG_766:g.151814del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1582+9del
ENST00000688602.1:c.2979+9del
ENST00000689936.1:c.2951+9del
ENST00000359596.8:c.14646+9del MANE Select	ENSP00000352608.2:n.14646+9del
ENST00000355481.8:c.14631+9del	ENSP00000347667.3:n.14631+9del
ENST00000359596.7:c.14646+9del	ENSP00000352608.2:n.14646+9del
ENST00000360985.7:c.14628+9del	ENSP00000354254.4:n.14628+9del
NM_000540.2:c.14646+9del , LRG_766t1:c.14646+9del	NP_000531.2:n.14646+9del
NM_001042723.1:c.14631+9del	NP_001036188.1:n.14631+9del
XM_006723317.1:c.14628+9del	XP_006723380.1:n.14628+9del
XM_006723319.1:c.14613+9del	XP_006723382.1:n.14613+9del
XM_011527204.1:c.14643+9del	XP_011525506.1:n.14643+9del
XM_011527205.1:c.14559+9del	XP_011525507.1:n.14559+9del
XM_006723317.2:c.14628+9del	XP_006723380.1:n.14628+9del
XM_006723319.2:c.14613+9del	XP_006723382.1:n.14613+9del
XM_011527205.2:c.14559+9del	XP_011525507.1:n.14559+9del
NM_000540.3:c.14646+9del MANE Select	NP_000531.2:n.14646+9del
NM_001042723.2:c.14631+9del	NP_001036188.1:n.14631+9del