Canonical Allele Identifier: CA2584908089

Gene: RYR1

Linked Data

• gnomAD v4: 19-38543466-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543469del , CM000681.2:g.38543469del	GRCh38
NC_000019.9:g.39034109del , CM000681.1:g.39034109del	GRCh37
NC_000019.8:g.43725949del	NCBI36
NG_008866.1:g.114770del , LRG_766:g.114770del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.188+34del
ENST00000689936.1:c.170+34del
ENST00000359596.8:c.11778+34del MANE Select	ENSP00000352608.2:n.11778+34del
ENST00000355481.8:c.11763+34del	ENSP00000347667.3:n.11763+34del
ENST00000359596.7:c.11778+34del	ENSP00000352608.2:n.11778+34del
ENST00000360985.7:c.11760+34del	ENSP00000354254.4:n.11760+34del
ENST00000593322.1:c.387+34del
ENST00000594335.5:c.5147+34del
NM_000540.2:c.11778+34del , LRG_766t1:c.11778+34del	NP_000531.2:n.11778+34del
NM_001042723.1:c.11763+34del	NP_001036188.1:n.11763+34del
XM_006723317.1:c.11760+34del	XP_006723380.1:n.11760+34del
XM_006723319.1:c.11745+34del	XP_006723382.1:n.11745+34del
XM_011527204.1:c.11775+34del	XP_011525506.1:n.11775+34del
XM_011527205.1:c.11778+34del	XP_011525507.1:n.11778+34del
XM_006723317.2:c.11760+34del	XP_006723380.1:n.11760+34del
XM_006723319.2:c.11745+34del	XP_006723382.1:n.11745+34del
XM_011527205.2:c.11778+34del	XP_011525507.1:n.11778+34del
NM_000540.3:c.11778+34del MANE Select	NP_000531.2:n.11778+34del
NM_001042723.2:c.11763+34del	NP_001036188.1:n.11763+34del