Canonical Allele Identifier: CA2335046147
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38485626C= , CM000681.2:g.38485626C= GRCh38
NC_000019.9:g.38976266C= , CM000681.1:g.38976266C= GRCh37
NC_000019.8:g.43668106C= NCBI36
NG_008866.1:g.56927C= , LRG_766:g.56927C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.4971C= ENSP00000471601.2:p.Asp1657=
ENST00000359596.8:c.4971C= MANE Select ENSP00000352608.2:p.Asp1657=
ENST00000355481.8:c.4971C= ENSP00000347667.3:p.Asp1657=
ENST00000359596.7:c.4971C= ENSP00000352608.2:p.Asp1657=
ENST00000360985.7:c.4968C= ENSP00000354254.4:p.Asp1656=
NM_000540.2:c.4971C= , LRG_766t1:c.4971C= NP_000531.2:p.Asp1657=
NM_001042723.1:c.4971C= NP_001036188.1:p.Asp1657=
XM_006723317.1:c.4971C= XP_006723380.1:p.Asp1657=
XM_006723319.1:c.4971C= XP_006723382.1:p.Asp1657=
XM_011527204.1:c.4968C= XP_011525506.1:p.Asp1656=
XM_011527205.1:c.4971C= XP_011525507.1:p.Asp1657=
XM_006723317.2:c.4971C= XP_006723380.1:p.Asp1657=
XM_006723319.2:c.4971C= XP_006723382.1:p.Asp1657=
XM_011527205.2:c.4971C= XP_011525507.1:p.Asp1657=
XR_001753735.1:n.5054C=
NM_000540.3:c.4971C= MANE Select NP_000531.2:p.Asp1657=
NM_001042723.2:c.4971C= NP_001036188.1:p.Asp1657=