Canonical Allele Identifier: CA2335091352
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38578078G= , CM000681.2:g.38578078G= GRCh38
NC_000019.9:g.39068718G= , CM000681.1:g.39068718G= GRCh37
NC_000019.8:g.43760558G= NCBI36
NG_008866.1:g.149379G= , LRG_766:g.149379G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1239+30G=
ENST00000688602.1:c.2636+30G=
ENST00000689936.1:c.2608+30G=
ENST00000359596.8:c.14303+30G= MANE Select ENSP00000352608.2:n.14303+30G=
ENST00000355481.8:c.14288+30G= ENSP00000347667.3:n.14288+30G=
ENST00000359596.7:c.14303+30G= ENSP00000352608.2:n.14303+30G=
ENST00000360985.7:c.14285+30G= ENSP00000354254.4:n.14285+30G=
NM_000540.2:c.14303+30G= , LRG_766t1:c.14303+30G= NP_000531.2:n.14303+30G=
NM_001042723.1:c.14288+30G= NP_001036188.1:n.14288+30G=
XM_006723317.1:c.14285+30G= XP_006723380.1:n.14285+30G=
XM_006723319.1:c.14270+30G= XP_006723382.1:n.14270+30G=
XM_011527204.1:c.14300+30G= XP_011525506.1:n.14300+30G=
XM_011527205.1:c.14216+30G= XP_011525507.1:n.14216+30G=
XM_006723317.2:c.14285+30G= XP_006723380.1:n.14285+30G=
XM_006723319.2:c.14270+30G= XP_006723382.1:n.14270+30G=
XM_011527205.2:c.14216+30G= XP_011525507.1:n.14216+30G=
NM_000540.3:c.14303+30G= MANE Select NP_000531.2:n.14303+30G=
NM_001042723.2:c.14288+30G= NP_001036188.1:n.14288+30G=