Canonical Allele Identifier: CA308127385

Gene: RYR1

Linked Data

• dbSNP Id: rs1023241959
• gnomAD v2: 19-39077897-T-A
• gnomAD v3: 19-38587257-T-A
• gnomAD v4: 19-38587257-T-A
• COSMIC: COSN1215321 ; COSN5760412
• MyVariant Identifiers: chr19:g.39077897T>A (hg19) ; chr19:g.38587257T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38587257T>A , CM000681.2:g.38587257T>A	GRCh38
NC_000019.9:g.39077897T>A , CM000681.1:g.39077897T>A	GRCh37
NC_000019.8:g.43769737T>A	NCBI36
NG_008866.1:g.158558T>A , LRG_766:g.158558T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1957+681T>A
ENST00000688602.1:c.3355-68T>A
ENST00000689936.1:c.3327-68T>A
ENST00000692547.1:n.415-68T>A
ENST00000359596.8:c.15022-68T>A MANE Select	ENSP00000352608.2:n.15022-68T>A
ENST00000355481.8:c.15007-68T>A	ENSP00000347667.3:n.15007-68T>A
ENST00000359596.7:c.15022-68T>A	ENSP00000352608.2:n.15022-68T>A
ENST00000360985.7:c.15004-68T>A	ENSP00000354254.4:n.15004-68T>A
NM_000540.2:c.15022-68T>A , LRG_766t1:c.15022-68T>A	NP_000531.2:n.15022-68T>A
NM_001042723.1:c.15007-68T>A	NP_001036188.1:n.15007-68T>A
XM_006723317.1:c.15004-68T>A	XP_006723380.1:n.15004-68T>A
XM_006723319.1:c.14989-68T>A	XP_006723382.1:n.14989-68T>A
XM_011527204.1:c.15019-68T>A	XP_011525506.1:n.15019-68T>A
XM_011527205.1:c.14935-68T>A	XP_011525507.1:n.14935-68T>A
XM_006723317.2:c.15004-68T>A	XP_006723380.1:n.15004-68T>A
XM_006723319.2:c.14989-68T>A	XP_006723382.1:n.14989-68T>A
XM_011527205.2:c.14935-68T>A	XP_011525507.1:n.14935-68T>A
NM_000540.3:c.15022-68T>A MANE Select	NP_000531.2:n.15022-68T>A
NM_001042723.2:c.15007-68T>A	NP_001036188.1:n.15007-68T>A