Canonical Allele Identifier: CA2584900657

Gene: RYR1

Linked Data

• gnomAD v4: 19-38502751-T-TGGGGCAGGCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38502759_38502760insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG , CM000681.2:g.38502759_38502760insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	GRCh38
NC_000019.9:g.38993399_38993400insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG , CM000681.1:g.38993399_38993400insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	GRCh37
NC_000019.8:g.43685239_43685240insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	NCBI36
NG_008866.1:g.74060_74061insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG , LRG_766:g.74060_74061insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	ENSP00000471601.2:n.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGG...
ENST00000359596.8:c.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG MANE Select	ENSP00000352608.2:n.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGG...
ENST00000355481.8:c.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	ENSP00000347667.3:n.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGG...
ENST00000359596.7:c.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	ENSP00000352608.2:n.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGG...
ENST00000360985.7:c.7832+32_7832+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	ENSP00000354254.4:n.7832+32_7832+33insCTTCAGGGTGGGGCAGGGGCAGG...
ENST00000594335.5:c.1287+32_1287+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG
NM_000540.2:c.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG , LRG_766t1:c.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	NP_000531.2:n.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGG...
NM_001042723.1:c.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	NP_001036188.1:n.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGC...
XM_006723317.1:c.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	XP_006723380.1:n.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGC...
XM_006723319.1:c.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	XP_006723382.1:n.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGC...
XM_011527204.1:c.7832+32_7832+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	XP_011525506.1:n.7832+32_7832+33insCTTCAGGGTGGGGCAGGGGCAGGGGC...
XM_011527205.1:c.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	XP_011525507.1:n.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGC...
XM_006723317.2:c.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	XP_006723380.1:n.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGC...
XM_006723319.2:c.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	XP_006723382.1:n.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGC...
XM_011527205.2:c.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	XP_011525507.1:n.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGC...
XR_001753735.1:n.7918+32_7918+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG
NM_000540.3:c.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG MANE Select	NP_000531.2:n.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGG...
NM_001042723.2:c.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGGGGCAGG	NP_001036188.1:n.7835+32_7835+33insCTTCAGGGTGGGGCAGGGGCAGGGGC...