Canonical Allele Identifier: CA405661212

Gene: RYR1

Linked Data

• gnomAD v4: 19-38543383-C-G
• MyVariant Identifiers: chr19:g.39034023C>G (hg19) ; chr19:g.38543383C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38543383C>G , CM000681.2:g.38543383C>G	GRCh38
NC_000019.9:g.39034023C>G , CM000681.1:g.39034023C>G	GRCh37
NC_000019.8:g.43725863C>G	NCBI36
NG_008866.1:g.114684C>G , LRG_766:g.114684C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688602.1:c.136C>G
ENST00000689936.1:c.118C>G
ENST00000359596.8:c.11726C>G MANE Select	ENSP00000352608.2:p.Thr3909Arg
ENST00000355481.8:c.11711C>G	ENSP00000347667.3:p.Thr3904Arg
ENST00000359596.7:c.11726C>G	ENSP00000352608.2:p.Thr3909Arg
ENST00000360985.7:c.11708C>G	ENSP00000354254.4:p.Thr3903Arg
ENST00000593322.1:c.335C>G
ENST00000594335.5:c.5095C>G
NM_000540.2:c.11726C>G , LRG_766t1:c.11726C>G	NP_000531.2:p.Thr3909Arg
NM_001042723.1:c.11711C>G	NP_001036188.1:p.Thr3904Arg
XM_006723317.1:c.11708C>G	XP_006723380.1:p.Thr3903Arg
XM_006723319.1:c.11693C>G	XP_006723382.1:p.Thr3898Arg
XM_011527204.1:c.11723C>G	XP_011525506.1:p.Thr3908Arg
XM_011527205.1:c.11726C>G	XP_011525507.1:p.Thr3909Arg
XM_006723317.2:c.11708C>G	XP_006723380.1:p.Thr3903Arg
XM_006723319.2:c.11693C>G	XP_006723382.1:p.Thr3898Arg
XM_011527205.2:c.11726C>G	XP_011525507.1:p.Thr3909Arg
NM_000540.3:c.11726C>G MANE Select	NP_000531.2:p.Thr3909Arg
NM_001042723.2:c.11711C>G	NP_001036188.1:p.Thr3904Arg