Canonical Allele Identifier: CA2335067450
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38528604G= , CM000681.2:g.38528604G= GRCh38
NC_000019.9:g.39019244G= , CM000681.1:g.39019244G= GRCh37
NC_000019.8:g.43711084G= NCBI36
NG_008866.1:g.99905G= , LRG_766:g.99905G=

Transcript Alleles

HGVS Amino-acid change
ENST00000599547.6:c.10882G= ENSP00000471601.2:n.10882G=
ENST00000359596.8:c.10943G= MANE Select ENSP00000352608.2:p.Arg3648=
ENST00000355481.8:c.10928G= ENSP00000347667.3:p.Arg3643=
ENST00000359596.7:c.10943G= ENSP00000352608.2:p.Arg3648=
ENST00000360985.7:c.10925G= ENSP00000354254.4:p.Arg3642=
ENST00000594335.5:c.4330G=
ENST00000599547.5:c.1750G=
ENST00000601514.5:c.224G= ENSP00000472497.1:p.Arg75=
NM_000540.2:c.10943G= , LRG_766t1:c.10943G= NP_000531.2:p.Arg3648=
NM_001042723.1:c.10928G= NP_001036188.1:p.Arg3643=
XM_006723317.1:c.10943G= XP_006723380.1:p.Arg3648=
XM_006723319.1:c.10928G= XP_006723382.1:p.Arg3643=
XM_011527204.1:c.10940G= XP_011525506.1:p.Arg3647=
XM_011527205.1:c.10943G= XP_011525507.1:p.Arg3648=
XM_006723317.2:c.10943G= XP_006723380.1:p.Arg3648=
XM_006723319.2:c.10928G= XP_006723382.1:p.Arg3643=
XM_011527205.2:c.10943G= XP_011525507.1:p.Arg3648=
NM_000540.3:c.10943G= MANE Select NP_000531.2:p.Arg3648=
NM_001042723.2:c.10928G= NP_001036188.1:p.Arg3643=