Canonical Allele Identifier: CA2335091312
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38578003C= , CM000681.2:g.38578003C= GRCh38
NC_000019.9:g.39068643C= , CM000681.1:g.39068643C= GRCh37
NC_000019.8:g.43760483C= NCBI36
NG_008866.1:g.149304C= , LRG_766:g.149304C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1194C=
ENST00000688602.1:c.2591C=
ENST00000689936.1:c.2563C=
ENST00000359596.8:c.14258C= MANE Select ENSP00000352608.2:p.Ala4753=
ENST00000355481.8:c.14243C= ENSP00000347667.3:p.Ala4748=
ENST00000359596.7:c.14258C= ENSP00000352608.2:p.Ala4753=
ENST00000360985.7:c.14240C= ENSP00000354254.4:p.Ala4747=
NM_000540.2:c.14258C= , LRG_766t1:c.14258C= NP_000531.2:p.Ala4753=
NM_001042723.1:c.14243C= NP_001036188.1:p.Ala4748=
XM_006723317.1:c.14240C= XP_006723380.1:p.Ala4747=
XM_006723319.1:c.14225C= XP_006723382.1:p.Ala4742=
XM_011527204.1:c.14255C= XP_011525506.1:p.Ala4752=
XM_011527205.1:c.14171C= XP_011525507.1:p.Ala4724=
XM_006723317.2:c.14240C= XP_006723380.1:p.Ala4747=
XM_006723319.2:c.14225C= XP_006723382.1:p.Ala4742=
XM_011527205.2:c.14171C= XP_011525507.1:p.Ala4724=
NM_000540.3:c.14258C= MANE Select NP_000531.2:p.Ala4753=
NM_001042723.2:c.14243C= NP_001036188.1:p.Ala4748=