Canonical Allele Identifier: CA405687858
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38580450C>A , CM000681.2:g.38580450C>A GRCh38
NC_000019.9:g.39071090C>A , CM000681.1:g.39071090C>A GRCh37
NC_000019.8:g.43762930C>A NCBI36
NG_008866.1:g.151751C>A , LRG_766:g.151751C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.1528C>A
ENST00000688602.1:c.2925C>A
ENST00000689936.1:c.2897C>A
ENST00000359596.8:c.14592C>A MANE Select ENSP00000352608.2:p.Tyr4864Ter
ENST00000355481.8:c.14577C>A ENSP00000347667.3:p.Tyr4859Ter
ENST00000359596.7:c.14592C>A ENSP00000352608.2:p.Tyr4864Ter
ENST00000360985.7:c.14574C>A ENSP00000354254.4:p.Tyr4858Ter
NM_000540.2:c.14592C>A , LRG_766t1:c.14592C>A NP_000531.2:p.Tyr4864Ter
NM_001042723.1:c.14577C>A NP_001036188.1:p.Tyr4859Ter
XM_006723317.1:c.14574C>A XP_006723380.1:p.Tyr4858Ter
XM_006723319.1:c.14559C>A XP_006723382.1:p.Tyr4853Ter
XM_011527204.1:c.14589C>A XP_011525506.1:p.Tyr4863Ter
XM_011527205.1:c.14505C>A XP_011525507.1:p.Tyr4835Ter
XM_006723317.2:c.14574C>A XP_006723380.1:p.Tyr4858Ter
XM_006723319.2:c.14559C>A XP_006723382.1:p.Tyr4853Ter
XM_011527205.2:c.14505C>A XP_011525507.1:p.Tyr4835Ter
NM_000540.3:c.14592C>A MANE Select NP_000531.2:p.Tyr4864Ter
NM_001042723.2:c.14577C>A NP_001036188.1:p.Tyr4859Ter