Canonical Allele Identifier: CA308125185

Gene: RYR1

Linked Data

• ClinVar Variation Id: 1210299
• ClinVar RCV Id: RCV001580390 ; RCV003319571
• dbSNP Id: rs118204423
• MyVariant Identifiers: chr19:g.38948179G>C (hg19) ; chr19:g.38457539G>C (hg38)
• ERepo: CA308125185/MONDO:0007783/012

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38457539G>C , CM000681.2:g.38457539G>C	GRCh38
NC_000019.9:g.38948179G>C , CM000681.1:g.38948179G>C	GRCh37
NC_000019.8:g.43640019G>C	NCBI36
NG_008866.1:g.28840G>C , LRG_766:g.28840G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000599547.6:c.1834G>C	ENSP00000471601.2:p.Ala612Pro
ENST00000359596.8:c.1834G>C MANE Select	ENSP00000352608.2:p.Ala612Pro
ENST00000355481.8:c.1834G>C	ENSP00000347667.3:p.Ala612Pro
ENST00000359596.7:c.1834G>C	ENSP00000352608.2:p.Ala612Pro
ENST00000360985.7:c.1834G>C	ENSP00000354254.4:p.Ala612Pro
NM_000540.2:c.1834G>C , LRG_766t1:c.1834G>C	NP_000531.2:p.Ala612Pro
NM_001042723.1:c.1834G>C	NP_001036188.1:p.Ala612Pro
XM_006723317.1:c.1834G>C	XP_006723380.1:p.Ala612Pro
XM_006723319.1:c.1834G>C	XP_006723382.1:p.Ala612Pro
XM_011527204.1:c.1831G>C	XP_011525506.1:p.Ala611Pro
XM_011527205.1:c.1834G>C	XP_011525507.1:p.Ala612Pro
XM_006723317.2:c.1834G>C	XP_006723380.1:p.Ala612Pro
XM_006723319.2:c.1834G>C	XP_006723382.1:p.Ala612Pro
XM_011527205.2:c.1834G>C	XP_011525507.1:p.Ala612Pro
XR_001753735.1:n.1917G>C
NM_000540.3:c.1834G>C MANE Select	NP_000531.2:p.Ala612Pro
NM_001042723.2:c.1834G>C	NP_001036188.1:p.Ala612Pro