Canonical Allele Identifier: CA405687629

Gene: RYR1

Linked Data

• ClinVar Variation Id: 1008044
• ClinVar RCV Id: RCV001305318
• dbSNP Id: rs1974146322
• MyVariant Identifiers: chr19:g.39071034G>C (hg19) ; chr19:g.38580394G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38580394G>C , CM000681.2:g.38580394G>C	GRCh38
NC_000019.9:g.39071034G>C , CM000681.1:g.39071034G>C	GRCh37
NC_000019.8:g.43762874G>C	NCBI36
NG_008866.1:g.151695G>C , LRG_766:g.151695G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593677.2:c.1472G>C
ENST00000688602.1:c.2869G>C
ENST00000689936.1:c.2841G>C
ENST00000359596.8:c.14536G>C MANE Select	ENSP00000352608.2:p.Ala4846Pro
ENST00000355481.8:c.14521G>C	ENSP00000347667.3:p.Ala4841Pro
ENST00000359596.7:c.14536G>C	ENSP00000352608.2:p.Ala4846Pro
ENST00000360985.7:c.14518G>C	ENSP00000354254.4:p.Ala4840Pro
NM_000540.2:c.14536G>C , LRG_766t1:c.14536G>C	NP_000531.2:p.Ala4846Pro
NM_001042723.1:c.14521G>C	NP_001036188.1:p.Ala4841Pro
XM_006723317.1:c.14518G>C	XP_006723380.1:p.Ala4840Pro
XM_006723319.1:c.14503G>C	XP_006723382.1:p.Ala4835Pro
XM_011527204.1:c.14533G>C	XP_011525506.1:p.Ala4845Pro
XM_011527205.1:c.14449G>C	XP_011525507.1:p.Ala4817Pro
XM_006723317.2:c.14518G>C	XP_006723380.1:p.Ala4840Pro
XM_006723319.2:c.14503G>C	XP_006723382.1:p.Ala4835Pro
XM_011527205.2:c.14449G>C	XP_011525507.1:p.Ala4817Pro
NM_000540.3:c.14536G>C MANE Select	NP_000531.2:p.Ala4846Pro
NM_001042723.2:c.14521G>C	NP_001036188.1:p.Ala4841Pro