Canonical Allele Identifier: CA882064629
Gene: RYR1 HGNC NCBI

Linked Data

dbSNP Id: rs1162969528

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38580342A>G , CM000681.2:g.38580342A>G GRCh38
NC_000019.9:g.39070982A>G , CM000681.1:g.39070982A>G GRCh37
NC_000019.8:g.43762822A>G NCBI36
NG_008866.1:g.151643A>G , LRG_766:g.151643A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.1448-28A>G
ENST00000688602.1:c.2845-28A>G
ENST00000689936.1:c.2817-28A>G
ENST00000359596.8:c.14512-28A>G MANE Select ENSP00000352608.2:n.14512-28A>G
ENST00000355481.8:c.14497-28A>G ENSP00000347667.3:n.14497-28A>G
ENST00000359596.7:c.14512-28A>G ENSP00000352608.2:n.14512-28A>G
ENST00000360985.7:c.14494-28A>G ENSP00000354254.4:n.14494-28A>G
NM_000540.2:c.14512-28A>G , LRG_766t1:c.14512-28A>G NP_000531.2:n.14512-28A>G
NM_001042723.1:c.14497-28A>G NP_001036188.1:n.14497-28A>G
XM_006723317.1:c.14494-28A>G XP_006723380.1:n.14494-28A>G
XM_006723319.1:c.14479-28A>G XP_006723382.1:n.14479-28A>G
XM_011527204.1:c.14509-28A>G XP_011525506.1:n.14509-28A>G
XM_011527205.1:c.14425-28A>G XP_011525507.1:n.14425-28A>G
XM_006723317.2:c.14494-28A>G XP_006723380.1:n.14494-28A>G
XM_006723319.2:c.14479-28A>G XP_006723382.1:n.14479-28A>G
XM_011527205.2:c.14425-28A>G XP_011525507.1:n.14425-28A>G
NM_000540.3:c.14512-28A>G MANE Select NP_000531.2:n.14512-28A>G
NM_001042723.2:c.14497-28A>G NP_001036188.1:n.14497-28A>G