Canonical Allele Identifier: CA2335091305
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38577989A= , CM000681.2:g.38577989A= GRCh38
NC_000019.9:g.39068629A= , CM000681.1:g.39068629A= GRCh37
NC_000019.8:g.43760469A= NCBI36
NG_008866.1:g.149290A= , LRG_766:g.149290A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1180A=
ENST00000688602.1:c.2577A=
ENST00000689936.1:c.2549A=
ENST00000359596.8:c.14244A= MANE Select ENSP00000352608.2:p.Thr4748=
ENST00000355481.8:c.14229A= ENSP00000347667.3:p.Thr4743=
ENST00000359596.7:c.14244A= ENSP00000352608.2:p.Thr4748=
ENST00000360985.7:c.14226A= ENSP00000354254.4:p.Thr4742=
NM_000540.2:c.14244A= , LRG_766t1:c.14244A= NP_000531.2:p.Thr4748=
NM_001042723.1:c.14229A= NP_001036188.1:p.Thr4743=
XM_006723317.1:c.14226A= XP_006723380.1:p.Thr4742=
XM_006723319.1:c.14211A= XP_006723382.1:p.Thr4737=
XM_011527204.1:c.14241A= XP_011525506.1:p.Thr4747=
XM_011527205.1:c.14157A= XP_011525507.1:p.Thr4719=
XM_006723317.2:c.14226A= XP_006723380.1:p.Thr4742=
XM_006723319.2:c.14211A= XP_006723382.1:p.Thr4737=
XM_011527205.2:c.14157A= XP_011525507.1:p.Thr4719=
NM_000540.3:c.14244A= MANE Select NP_000531.2:p.Thr4748=
NM_001042723.2:c.14229A= NP_001036188.1:p.Thr4743=