Canonical Allele Identifier: CA2335092390
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38580285T= , CM000681.2:g.38580285T= GRCh38
NC_000019.9:g.39070925T= , CM000681.1:g.39070925T= GRCh37
NC_000019.8:g.43762765T= NCBI36
NG_008866.1:g.151586T= , LRG_766:g.151586T=

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.1448-85T=
ENST00000688602.1:c.2845-85T=
ENST00000689936.1:c.2817-85T=
ENST00000359596.8:c.14512-85T= MANE Select ENSP00000352608.2:n.14512-85T=
ENST00000355481.8:c.14497-85T= ENSP00000347667.3:n.14497-85T=
ENST00000359596.7:c.14512-85T= ENSP00000352608.2:n.14512-85T=
ENST00000360985.7:c.14494-85T= ENSP00000354254.4:n.14494-85T=
NM_000540.2:c.14512-85T= , LRG_766t1:c.14512-85T= NP_000531.2:n.14512-85T=
NM_001042723.1:c.14497-85T= NP_001036188.1:n.14497-85T=
XM_006723317.1:c.14494-85T= XP_006723380.1:n.14494-85T=
XM_006723319.1:c.14479-85T= XP_006723382.1:n.14479-85T=
XM_011527204.1:c.14509-85T= XP_011525506.1:n.14509-85T=
XM_011527205.1:c.14425-85T= XP_011525507.1:n.14425-85T=
XM_006723317.2:c.14494-85T= XP_006723380.1:n.14494-85T=
XM_006723319.2:c.14479-85T= XP_006723382.1:n.14479-85T=
XM_011527205.2:c.14425-85T= XP_011525507.1:n.14425-85T=
NM_000540.3:c.14512-85T= MANE Select NP_000531.2:n.14512-85T=
NM_001042723.2:c.14497-85T= NP_001036188.1:n.14497-85T=