Canonical Allele Identifier: CA2584894089

Gene: RYR1

Linked Data

• gnomAD v4: 19-38455571-CAGAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38455572_38455575del , CM000681.2:g.38455572_38455575del	GRCh38
NC_000019.9:g.38946212_38946215del , CM000681.1:g.38946212_38946215del	GRCh37
NC_000019.8:g.43638052_43638055del	NCBI36
NG_008866.1:g.26873_26876del , LRG_766:g.26873_26876del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.1672+26_1672+29del	ENSP00000471601.2:n.1672+26_1672+29del
ENST00000359596.8:c.1672+26_1672+29del MANE Select	ENSP00000352608.2:n.1672+26_1672+29del
ENST00000355481.8:c.1672+26_1672+29del	ENSP00000347667.3:n.1672+26_1672+29del
ENST00000359596.7:c.1672+26_1672+29del	ENSP00000352608.2:n.1672+26_1672+29del
ENST00000360985.7:c.1672+26_1672+29del	ENSP00000354254.4:n.1672+26_1672+29del
NM_000540.2:c.1672+26_1672+29del , LRG_766t1:c.1672+26_1672+29del	NP_000531.2:n.1672+26_1672+29del
NM_001042723.1:c.1672+26_1672+29del	NP_001036188.1:n.1672+26_1672+29del
XM_006723317.1:c.1672+26_1672+29del	XP_006723380.1:n.1672+26_1672+29del
XM_006723319.1:c.1672+26_1672+29del	XP_006723382.1:n.1672+26_1672+29del
XM_011527204.1:c.1669+26_1669+29del	XP_011525506.1:n.1669+26_1669+29del
XM_011527205.1:c.1672+26_1672+29del	XP_011525507.1:n.1672+26_1672+29del
XM_006723317.2:c.1672+26_1672+29del	XP_006723380.1:n.1672+26_1672+29del
XM_006723319.2:c.1672+26_1672+29del	XP_006723382.1:n.1672+26_1672+29del
XM_011527205.2:c.1672+26_1672+29del	XP_011525507.1:n.1672+26_1672+29del
XR_001753735.1:n.1755+26_1755+29del
NM_000540.3:c.1672+26_1672+29del MANE Select	NP_000531.2:n.1672+26_1672+29del
NM_001042723.2:c.1672+26_1672+29del	NP_001036188.1:n.1672+26_1672+29del