Canonical Allele Identifier: CA072972

Gene: RYR1

Linked Data

• ClinVar Variation Id: 256579
• ClinVar RCV Id: RCV000244481
• dbSNP Id: rs374612710
• ExAC: 19:39001096 C / T
• gnomAD v2: 19-39001096-C-T
• gnomAD v3: 19-38510456-C-T
• gnomAD v4: 19-38510456-C-T
• MyVariant Identifiers: chr19:g.39001096C>T (hg19) ; chr19:g.38510456C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38510456C>T , CM000681.2:g.38510456C>T	GRCh38
NC_000019.9:g.39001096C>T , CM000681.1:g.39001096C>T	GRCh37
NC_000019.8:g.43692936C>T	NCBI36
NG_008866.1:g.81757C>T , LRG_766:g.81757C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.8933-42C>T	ENSP00000471601.2:n.8933-42C>T
ENST00000359596.8:c.8933-42C>T MANE Select	ENSP00000352608.2:n.8933-42C>T
ENST00000355481.8:c.8933-42C>T	ENSP00000347667.3:n.8933-42C>T
ENST00000359596.7:c.8933-42C>T	ENSP00000352608.2:n.8933-42C>T
ENST00000360985.7:c.8930-42C>T	ENSP00000354254.4:n.8930-42C>T
ENST00000594335.5:c.2385-42C>T
NM_000540.2:c.8933-42C>T , LRG_766t1:c.8933-42C>T	NP_000531.2:n.8933-42C>T
NM_001042723.1:c.8933-42C>T	NP_001036188.1:n.8933-42C>T
XM_006723317.1:c.8933-42C>T	XP_006723380.1:n.8933-42C>T
XM_006723319.1:c.8933-42C>T	XP_006723382.1:n.8933-42C>T
XM_011527204.1:c.8930-42C>T	XP_011525506.1:n.8930-42C>T
XM_011527205.1:c.8933-42C>T	XP_011525507.1:n.8933-42C>T
XM_006723317.2:c.8933-42C>T	XP_006723380.1:n.8933-42C>T
XM_006723319.2:c.8933-42C>T	XP_006723382.1:n.8933-42C>T
XM_011527205.2:c.8933-42C>T	XP_011525507.1:n.8933-42C>T
XR_001753735.1:n.9016-42C>T
NM_000540.3:c.8933-42C>T MANE Select	NP_000531.2:n.8933-42C>T
NM_001042723.2:c.8933-42C>T	NP_001036188.1:n.8933-42C>T