Canonical Allele Identifier: CA2584910301

Gene: RYR1

Linked Data

• gnomAD v4: 19-38573147-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38573150del , CM000681.2:g.38573150del	GRCh38
NC_000019.9:g.39063790del , CM000681.1:g.39063790del	GRCh37
NC_000019.8:g.43755630del	NCBI36
NG_008866.1:g.144451del , LRG_766:g.144451del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.935-27del
ENST00000688602.1:c.2332-27del
ENST00000689936.1:c.2304-27del
ENST00000359596.8:c.13999-27del MANE Select	ENSP00000352608.2:n.13999-27del
ENST00000355481.8:c.13984-27del	ENSP00000347667.3:n.13984-27del
ENST00000359596.7:c.13999-27del	ENSP00000352608.2:n.13999-27del
ENST00000360985.7:c.13981-27del	ENSP00000354254.4:n.13981-27del
NM_000540.2:c.13999-27del , LRG_766t1:c.13999-27del	NP_000531.2:n.13999-27del
NM_001042723.1:c.13984-27del	NP_001036188.1:n.13984-27del
XM_006723317.1:c.13981-27del	XP_006723380.1:n.13981-27del
XM_006723319.1:c.13966-27del	XP_006723382.1:n.13966-27del
XM_011527204.1:c.13996-27del	XP_011525506.1:n.13996-27del
XM_011527205.1:c.13912-27del	XP_011525507.1:n.13912-27del
XM_006723317.2:c.13981-27del	XP_006723380.1:n.13981-27del
XM_006723319.2:c.13966-27del	XP_006723382.1:n.13966-27del
XM_011527205.2:c.13912-27del	XP_011525507.1:n.13912-27del
NM_000540.3:c.13999-27del MANE Select	NP_000531.2:n.13999-27del
NM_001042723.2:c.13984-27del	NP_001036188.1:n.13984-27del