Canonical Allele Identifier: CA2335061923
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38517226G= , CM000681.2:g.38517226G= GRCh38
NC_000019.9:g.39007866G= , CM000681.1:g.39007866G= GRCh37
NC_000019.8:g.43699706G= NCBI36
NG_008866.1:g.88527G= , LRG_766:g.88527G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.9625-133G= ENSP00000471601.2:n.9625-133G=
ENST00000359596.8:c.9686-133G= MANE Select ENSP00000352608.2:n.9686-133G=
ENST00000355481.8:c.9686-133G= ENSP00000347667.3:n.9686-133G=
ENST00000359596.7:c.9686-133G= ENSP00000352608.2:n.9686-133G=
ENST00000360985.7:c.9683-133G= ENSP00000354254.4:n.9683-133G=
ENST00000594335.5:c.3088-133G=
ENST00000599547.5:c.493-133G=
NM_000540.2:c.9686-133G= , LRG_766t1:c.9686-133G= NP_000531.2:n.9686-133G=
NM_001042723.1:c.9686-133G= NP_001036188.1:n.9686-133G=
XM_006723317.1:c.9686-133G= XP_006723380.1:n.9686-133G=
XM_006723319.1:c.9686-133G= XP_006723382.1:n.9686-133G=
XM_011527204.1:c.9683-133G= XP_011525506.1:n.9683-133G=
XM_011527205.1:c.9686-133G= XP_011525507.1:n.9686-133G=
XM_006723317.2:c.9686-133G= XP_006723380.1:n.9686-133G=
XM_006723319.2:c.9686-133G= XP_006723382.1:n.9686-133G=
XM_011527205.2:c.9686-133G= XP_011525507.1:n.9686-133G=
XR_001753735.1:n.9719-133G=
NM_000540.3:c.9686-133G= MANE Select NP_000531.2:n.9686-133G=
NM_001042723.2:c.9686-133G= NP_001036188.1:n.9686-133G=