Canonical Allele Identifier: CA2335091279
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38577934G= , CM000681.2:g.38577934G= GRCh38
NC_000019.9:g.39068574G= , CM000681.1:g.39068574G= GRCh37
NC_000019.8:g.43760414G= NCBI36
NG_008866.1:g.149235G= , LRG_766:g.149235G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1125G=
ENST00000688602.1:c.2522G=
ENST00000689936.1:c.2494G=
ENST00000359596.8:c.14189G= MANE Select ENSP00000352608.2:p.Gly4730=
ENST00000355481.8:c.14174G= ENSP00000347667.3:p.Gly4725=
ENST00000359596.7:c.14189G= ENSP00000352608.2:p.Gly4730=
ENST00000360985.7:c.14171G= ENSP00000354254.4:p.Gly4724=
NM_000540.2:c.14189G= , LRG_766t1:c.14189G= NP_000531.2:p.Gly4730=
NM_001042723.1:c.14174G= NP_001036188.1:p.Gly4725=
XM_006723317.1:c.14171G= XP_006723380.1:p.Gly4724=
XM_006723319.1:c.14156G= XP_006723382.1:p.Gly4719=
XM_011527204.1:c.14186G= XP_011525506.1:p.Gly4729=
XM_011527205.1:c.14102G= XP_011525507.1:p.Gly4701=
XM_006723317.2:c.14171G= XP_006723380.1:p.Gly4724=
XM_006723319.2:c.14156G= XP_006723382.1:p.Gly4719=
XM_011527205.2:c.14102G= XP_011525507.1:p.Gly4701=
NM_000540.3:c.14189G= MANE Select NP_000531.2:p.Gly4730=
NM_001042723.2:c.14174G= NP_001036188.1:p.Gly4725=