Canonical Allele Identifier: CA2335052948
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38499811C= , CM000681.2:g.38499811C= GRCh38
NC_000019.9:g.38990451C= , CM000681.1:g.38990451C= GRCh37
NC_000019.8:g.43682291C= NCBI36
NG_008866.1:g.71112C= , LRG_766:g.71112C=

Transcript Alleles

HGVS Amino-acid change
ENST00000599547.6:c.7204C= ENSP00000471601.2:p.Arg2402=
ENST00000359596.8:c.7204C= MANE Select ENSP00000352608.2:p.Arg2402=
ENST00000355481.8:c.7204C= ENSP00000347667.3:p.Arg2402=
ENST00000359596.7:c.7204C= ENSP00000352608.2:p.Arg2402=
ENST00000360985.7:c.7201C= ENSP00000354254.4:p.Arg2401=
ENST00000594335.5:c.656C=
NM_000540.2:c.7204C= , LRG_766t1:c.7204C= NP_000531.2:p.Arg2402=
NM_001042723.1:c.7204C= NP_001036188.1:p.Arg2402=
XM_006723317.1:c.7204C= XP_006723380.1:p.Arg2402=
XM_006723319.1:c.7204C= XP_006723382.1:p.Arg2402=
XM_011527204.1:c.7201C= XP_011525506.1:p.Arg2401=
XM_011527205.1:c.7204C= XP_011525507.1:p.Arg2402=
XM_006723317.2:c.7204C= XP_006723380.1:p.Arg2402=
XM_006723319.2:c.7204C= XP_006723382.1:p.Arg2402=
XM_011527205.2:c.7204C= XP_011525507.1:p.Arg2402=
XR_001753735.1:n.7287C=
NM_000540.3:c.7204C= MANE Select NP_000531.2:p.Arg2402=
NM_001042723.2:c.7204C= NP_001036188.1:p.Arg2402=