Canonical Allele Identifier: CA2335091298
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38577973G= , CM000681.2:g.38577973G= GRCh38
NC_000019.9:g.39068613G= , CM000681.1:g.39068613G= GRCh37
NC_000019.8:g.43760453G= NCBI36
NG_008866.1:g.149274G= , LRG_766:g.149274G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1164G=
ENST00000688602.1:c.2561G=
ENST00000689936.1:c.2533G=
ENST00000359596.8:c.14228G= MANE Select ENSP00000352608.2:p.Gly4743=
ENST00000355481.8:c.14213G= ENSP00000347667.3:p.Gly4738=
ENST00000359596.7:c.14228G= ENSP00000352608.2:p.Gly4743=
ENST00000360985.7:c.14210G= ENSP00000354254.4:p.Gly4737=
NM_000540.2:c.14228G= , LRG_766t1:c.14228G= NP_000531.2:p.Gly4743=
NM_001042723.1:c.14213G= NP_001036188.1:p.Gly4738=
XM_006723317.1:c.14210G= XP_006723380.1:p.Gly4737=
XM_006723319.1:c.14195G= XP_006723382.1:p.Gly4732=
XM_011527204.1:c.14225G= XP_011525506.1:p.Gly4742=
XM_011527205.1:c.14141G= XP_011525507.1:p.Gly4714=
XM_006723317.2:c.14210G= XP_006723380.1:p.Gly4737=
XM_006723319.2:c.14195G= XP_006723382.1:p.Gly4732=
XM_011527205.2:c.14141G= XP_011525507.1:p.Gly4714=
NM_000540.3:c.14228G= MANE Select NP_000531.2:p.Gly4743=
NM_001042723.2:c.14213G= NP_001036188.1:p.Gly4738=