Canonical Allele Identifier: CA2335091286
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38577944C= , CM000681.2:g.38577944C= GRCh38
NC_000019.9:g.39068584C= , CM000681.1:g.39068584C= GRCh37
NC_000019.8:g.43760424C= NCBI36
NG_008866.1:g.149245C= , LRG_766:g.149245C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1135C=
ENST00000688602.1:c.2532C=
ENST00000689936.1:c.2504C=
ENST00000359596.8:c.14199C= MANE Select ENSP00000352608.2:p.Tyr4733=
ENST00000355481.8:c.14184C= ENSP00000347667.3:p.Tyr4728=
ENST00000359596.7:c.14199C= ENSP00000352608.2:p.Tyr4733=
ENST00000360985.7:c.14181C= ENSP00000354254.4:p.Tyr4727=
NM_000540.2:c.14199C= , LRG_766t1:c.14199C= NP_000531.2:p.Tyr4733=
NM_001042723.1:c.14184C= NP_001036188.1:p.Tyr4728=
XM_006723317.1:c.14181C= XP_006723380.1:p.Tyr4727=
XM_006723319.1:c.14166C= XP_006723382.1:p.Tyr4722=
XM_011527204.1:c.14196C= XP_011525506.1:p.Tyr4732=
XM_011527205.1:c.14112C= XP_011525507.1:p.Tyr4704=
XM_006723317.2:c.14181C= XP_006723380.1:p.Tyr4727=
XM_006723319.2:c.14166C= XP_006723382.1:p.Tyr4722=
XM_011527205.2:c.14112C= XP_011525507.1:p.Tyr4704=
NM_000540.3:c.14199C= MANE Select NP_000531.2:p.Tyr4733=
NM_001042723.2:c.14184C= NP_001036188.1:p.Tyr4728=