Canonical Allele Identifier: CA2335091353
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38578079G= , CM000681.2:g.38578079G= GRCh38
NC_000019.9:g.39068719G= , CM000681.1:g.39068719G= GRCh37
NC_000019.8:g.43760559G= NCBI36
NG_008866.1:g.149380G= , LRG_766:g.149380G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1239+31G=
ENST00000688602.1:c.2636+31G=
ENST00000689936.1:c.2608+31G=
ENST00000359596.8:c.14303+31G= MANE Select ENSP00000352608.2:n.14303+31G=
ENST00000355481.8:c.14288+31G= ENSP00000347667.3:n.14288+31G=
ENST00000359596.7:c.14303+31G= ENSP00000352608.2:n.14303+31G=
ENST00000360985.7:c.14285+31G= ENSP00000354254.4:n.14285+31G=
NM_000540.2:c.14303+31G= , LRG_766t1:c.14303+31G= NP_000531.2:n.14303+31G=
NM_001042723.1:c.14288+31G= NP_001036188.1:n.14288+31G=
XM_006723317.1:c.14285+31G= XP_006723380.1:n.14285+31G=
XM_006723319.1:c.14270+31G= XP_006723382.1:n.14270+31G=
XM_011527204.1:c.14300+31G= XP_011525506.1:n.14300+31G=
XM_011527205.1:c.14216+31G= XP_011525507.1:n.14216+31G=
XM_006723317.2:c.14285+31G= XP_006723380.1:n.14285+31G=
XM_006723319.2:c.14270+31G= XP_006723382.1:n.14270+31G=
XM_011527205.2:c.14216+31G= XP_011525507.1:n.14216+31G=
NM_000540.3:c.14303+31G= MANE Select NP_000531.2:n.14303+31G=
NM_001042723.2:c.14288+31G= NP_001036188.1:n.14288+31G=