Canonical Allele Identifier: CA2584910348

Gene: RYR1

Linked Data

• gnomAD v4: 19-38573401-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38573403del , CM000681.2:g.38573403del	GRCh38
NC_000019.9:g.39064043del , CM000681.1:g.39064043del	GRCh37
NC_000019.8:g.43755883del	NCBI36
NG_008866.1:g.144704del , LRG_766:g.144704del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1065+96del
ENST00000688602.1:c.2462+96del
ENST00000689936.1:c.2434+96del
ENST00000359596.8:c.14129+96del MANE Select	ENSP00000352608.2:n.14129+96del
ENST00000355481.8:c.14114+96del	ENSP00000347667.3:n.14114+96del
ENST00000359596.7:c.14129+96del	ENSP00000352608.2:n.14129+96del
ENST00000360985.7:c.14111+96del	ENSP00000354254.4:n.14111+96del
NM_000540.2:c.14129+96del , LRG_766t1:c.14129+96del	NP_000531.2:n.14129+96del
NM_001042723.1:c.14114+96del	NP_001036188.1:n.14114+96del
XM_006723317.1:c.14111+96del	XP_006723380.1:n.14111+96del
XM_006723319.1:c.14096+96del	XP_006723382.1:n.14096+96del
XM_011527204.1:c.14126+96del	XP_011525506.1:n.14126+96del
XM_011527205.1:c.14042+96del	XP_011525507.1:n.14042+96del
XM_006723317.2:c.14111+96del	XP_006723380.1:n.14111+96del
XM_006723319.2:c.14096+96del	XP_006723382.1:n.14096+96del
XM_011527205.2:c.14042+96del	XP_011525507.1:n.14042+96del
NM_000540.3:c.14129+96del MANE Select	NP_000531.2:n.14129+96del
NM_001042723.2:c.14114+96del	NP_001036188.1:n.14114+96del