Canonical Allele Identifier: CA2335074512
Gene: RYR1 HGNC NCBI

Linked Data

dbSNP Id: rs1600988900

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38543754G>A , CM000681.2:g.38543754G>A GRCh38
NC_000019.9:g.39034394G>A , CM000681.1:g.39034394G>A GRCh37
NC_000019.8:g.43726234G>A NCBI36
NG_008866.1:g.115055G>A , LRG_766:g.115055G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000688602.1:c.318-17G>A
ENST00000689936.1:c.300-17G>A
ENST00000359596.8:c.11908-17G>A MANE Select ENSP00000352608.2:n.11908-17G>A
ENST00000355481.8:c.11893-17G>A ENSP00000347667.3:n.11893-17G>A
ENST00000359596.7:c.11908-17G>A ENSP00000352608.2:n.11908-17G>A
ENST00000360985.7:c.11890-17G>A ENSP00000354254.4:n.11890-17G>A
ENST00000593322.1:c.517-17G>A
ENST00000594335.5:c.5277-17G>A
NM_000540.2:c.11908-17G>A , LRG_766t1:c.11908-17G>A NP_000531.2:n.11908-17G>A
NM_001042723.1:c.11893-17G>A NP_001036188.1:n.11893-17G>A
XM_006723317.1:c.11890-17G>A XP_006723380.1:n.11890-17G>A
XM_006723319.1:c.11875-17G>A XP_006723382.1:n.11875-17G>A
XM_011527204.1:c.11905-17G>A XP_011525506.1:n.11905-17G>A
XM_011527205.1:c.11908-17G>A XP_011525507.1:n.11908-17G>A
XM_006723317.2:c.11890-17G>A XP_006723380.1:n.11890-17G>A
XM_006723319.2:c.11875-17G>A XP_006723382.1:n.11875-17G>A
XM_011527205.2:c.11908-17G>A XP_011525507.1:n.11908-17G>A
NM_000540.3:c.11908-17G>A MANE Select NP_000531.2:n.11908-17G>A
NM_001042723.2:c.11893-17G>A NP_001036188.1:n.11893-17G>A