Canonical Allele Identifier: CA2335092536
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38580542T= , CM000681.2:g.38580542T= GRCh38
NC_000019.9:g.39071182T= , CM000681.1:g.39071182T= GRCh37
NC_000019.8:g.43763022T= NCBI36
NG_008866.1:g.151843T= , LRG_766:g.151843T=

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.1582+38T=
ENST00000688602.1:c.2979+38T=
ENST00000689936.1:c.2951+38T=
ENST00000359596.8:c.14646+38T= MANE Select ENSP00000352608.2:n.14646+38T=
ENST00000355481.8:c.14631+38T= ENSP00000347667.3:n.14631+38T=
ENST00000359596.7:c.14646+38T= ENSP00000352608.2:n.14646+38T=
ENST00000360985.7:c.14628+38T= ENSP00000354254.4:n.14628+38T=
NM_000540.2:c.14646+38T= , LRG_766t1:c.14646+38T= NP_000531.2:n.14646+38T=
NM_001042723.1:c.14631+38T= NP_001036188.1:n.14631+38T=
XM_006723317.1:c.14628+38T= XP_006723380.1:n.14628+38T=
XM_006723319.1:c.14613+38T= XP_006723382.1:n.14613+38T=
XM_011527204.1:c.14643+38T= XP_011525506.1:n.14643+38T=
XM_011527205.1:c.14559+38T= XP_011525507.1:n.14559+38T=
XM_006723317.2:c.14628+38T= XP_006723380.1:n.14628+38T=
XM_006723319.2:c.14613+38T= XP_006723382.1:n.14613+38T=
XM_011527205.2:c.14559+38T= XP_011525507.1:n.14559+38T=
NM_000540.3:c.14646+38T= MANE Select NP_000531.2:n.14646+38T=
NM_001042723.2:c.14631+38T= NP_001036188.1:n.14631+38T=