Canonical Allele Identifier: CA2335054479
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502739_38502751delinsCAGGCTTCAGGGT , CM000681.2:g.38502739_38502751delinsCAGGCTTCAGGGT GRCh38
NC_000019.9:g.38993379_38993391delinsCAGGCTTCAGGGT , CM000681.1:g.38993379_38993391delinsCAGGCTTCAGGGT GRCh37
NC_000019.8:g.43685219_43685231delinsCAGGCTTCAGGGT NCBI36
NG_008866.1:g.74040_74052delinsCAGGCTTCAGGGT , LRG_766:g.74040_74052delinsCAGGCTTCAGGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7835+12_7835+24delinsCAGGCTTCAGGGT ENSP00000471601.2:n.7835+12_7835+24delinsCAGGCTTCAGGGT
ENST00000359596.8:c.7835+12_7835+24delinsCAGGCTTCAGGGT MANE Select ENSP00000352608.2:n.7835+12_7835+24delinsCAGGCTTCAGGGT
ENST00000355481.8:c.7835+12_7835+24delinsCAGGCTTCAGGGT ENSP00000347667.3:n.7835+12_7835+24delinsCAGGCTTCAGGGT
ENST00000359596.7:c.7835+12_7835+24delinsCAGGCTTCAGGGT ENSP00000352608.2:n.7835+12_7835+24delinsCAGGCTTCAGGGT
ENST00000360985.7:c.7832+12_7832+24delinsCAGGCTTCAGGGT ENSP00000354254.4:n.7832+12_7832+24delinsCAGGCTTCAGGGT
ENST00000594335.5:c.1287+12_1287+24delinsCAGGCTTCAGGGT
NM_000540.2:c.7835+12_7835+24delinsCAGGCTTCAGGGT , LRG_766t1:c.7835+12_7835+24delinsCAGGCTTCAGGGT NP_000531.2:n.7835+12_7835+24delinsCAGGCTTCAGGGT
NM_001042723.1:c.7835+12_7835+24delinsCAGGCTTCAGGGT NP_001036188.1:n.7835+12_7835+24delinsCAGGCTTCAGGGT
XM_006723317.1:c.7835+12_7835+24delinsCAGGCTTCAGGGT XP_006723380.1:n.7835+12_7835+24delinsCAGGCTTCAGGGT
XM_006723319.1:c.7835+12_7835+24delinsCAGGCTTCAGGGT XP_006723382.1:n.7835+12_7835+24delinsCAGGCTTCAGGGT
XM_011527204.1:c.7832+12_7832+24delinsCAGGCTTCAGGGT XP_011525506.1:n.7832+12_7832+24delinsCAGGCTTCAGGGT
XM_011527205.1:c.7835+12_7835+24delinsCAGGCTTCAGGGT XP_011525507.1:n.7835+12_7835+24delinsCAGGCTTCAGGGT
XM_006723317.2:c.7835+12_7835+24delinsCAGGCTTCAGGGT XP_006723380.1:n.7835+12_7835+24delinsCAGGCTTCAGGGT
XM_006723319.2:c.7835+12_7835+24delinsCAGGCTTCAGGGT XP_006723382.1:n.7835+12_7835+24delinsCAGGCTTCAGGGT
XM_011527205.2:c.7835+12_7835+24delinsCAGGCTTCAGGGT XP_011525507.1:n.7835+12_7835+24delinsCAGGCTTCAGGGT
XR_001753735.1:n.7918+12_7918+24delinsCAGGCTTCAGGGT
NM_000540.3:c.7835+12_7835+24delinsCAGGCTTCAGGGT MANE Select NP_000531.2:n.7835+12_7835+24delinsCAGGCTTCAGGGT
NM_001042723.2:c.7835+12_7835+24delinsCAGGCTTCAGGGT NP_001036188.1:n.7835+12_7835+24delinsCAGGCTTCAGGGT