Canonical Allele Identifier: CA405673376
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38565411G>A , CM000681.2:g.38565411G>A GRCh38
NC_000019.9:g.39056051G>A , CM000681.1:g.39056051G>A GRCh37
NC_000019.8:g.43747891G>A NCBI36
NG_008866.1:g.136712G>A , LRG_766:g.136712G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.13G>A
ENST00000688602.1:c.1487G>A
ENST00000689936.1:c.1469G>A
ENST00000359596.8:c.13077G>A MANE Select ENSP00000352608.2:p.Trp4359Ter
ENST00000355481.8:c.13062G>A ENSP00000347667.3:p.Trp4354Ter
ENST00000359596.7:c.13077G>A ENSP00000352608.2:p.Trp4359Ter
ENST00000360985.7:c.13059G>A ENSP00000354254.4:p.Trp4353Ter
NM_000540.2:c.13077G>A , LRG_766t1:c.13077G>A NP_000531.2:p.Trp4359Ter
NM_001042723.1:c.13062G>A NP_001036188.1:p.Trp4354Ter
XM_006723317.1:c.13059G>A XP_006723380.1:p.Trp4353Ter
XM_006723319.1:c.13044G>A XP_006723382.1:p.Trp4348Ter
XM_011527204.1:c.13074G>A XP_011525506.1:p.Trp4358Ter
XM_011527205.1:c.13077G>A XP_011525507.1:p.Trp4359Ter
XM_006723317.2:c.13059G>A XP_006723380.1:p.Trp4353Ter
XM_006723319.2:c.13044G>A XP_006723382.1:p.Trp4348Ter
XM_011527205.2:c.13077G>A XP_011525507.1:p.Trp4359Ter
NM_000540.3:c.13077G>A MANE Select NP_000531.2:p.Trp4359Ter
NM_001042723.2:c.13062G>A NP_001036188.1:p.Trp4354Ter