Canonical Allele Identifier: CA405673905

Gene: RYR1

Linked Data

• ClinVar Variation Id: 1352926
• ClinVar RCV Id: RCV002040045 ; RCV002489947
• dbSNP Id: rs1413644550
• gnomAD v2: 19-39056142-G-C
• gnomAD v3: 19-38565502-G-C
• gnomAD v4: 19-38565502-G-C
• MyVariant Identifiers: chr19:g.39056142G>C (hg19) ; chr19:g.38565502G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38565502G>C , CM000681.2:g.38565502G>C	GRCh38
NC_000019.9:g.39056142G>C , CM000681.1:g.39056142G>C	GRCh37
NC_000019.8:g.43747982G>C	NCBI36
NG_008866.1:g.136803G>C , LRG_766:g.136803G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.104G>C
ENST00000688602.1:c.1578G>C
ENST00000689936.1:c.1560G>C
ENST00000359596.8:c.13168G>C MANE Select	ENSP00000352608.2:p.Glu4390Gln
ENST00000355481.8:c.13153G>C	ENSP00000347667.3:p.Glu4385Gln
ENST00000359596.7:c.13168G>C	ENSP00000352608.2:p.Glu4390Gln
ENST00000360985.7:c.13150G>C	ENSP00000354254.4:p.Glu4384Gln
NM_000540.2:c.13168G>C , LRG_766t1:c.13168G>C	NP_000531.2:p.Glu4390Gln
NM_001042723.1:c.13153G>C	NP_001036188.1:p.Glu4385Gln
XM_006723317.1:c.13150G>C	XP_006723380.1:p.Glu4384Gln
XM_006723319.1:c.13135G>C	XP_006723382.1:p.Glu4379Gln
XM_011527204.1:c.13165G>C	XP_011525506.1:p.Glu4389Gln
XM_011527205.1:c.13168G>C	XP_011525507.1:p.Glu4390Gln
XM_006723317.2:c.13150G>C	XP_006723380.1:p.Glu4384Gln
XM_006723319.2:c.13135G>C	XP_006723382.1:p.Glu4379Gln
XM_011527205.2:c.13168G>C	XP_011525507.1:p.Glu4390Gln
NM_000540.3:c.13168G>C MANE Select	NP_000531.2:p.Glu4390Gln
NM_001042723.2:c.13153G>C	NP_001036188.1:p.Glu4385Gln