Canonical Allele Identifier: CA2335091314
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38578008A= , CM000681.2:g.38578008A= GRCh38
NC_000019.9:g.39068648A= , CM000681.1:g.39068648A= GRCh37
NC_000019.8:g.43760488A= NCBI36
NG_008866.1:g.149309A= , LRG_766:g.149309A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1199A=
ENST00000688602.1:c.2596A=
ENST00000689936.1:c.2568A=
ENST00000359596.8:c.14263A= MANE Select ENSP00000352608.2:p.Asn4755=
ENST00000355481.8:c.14248A= ENSP00000347667.3:p.Asn4750=
ENST00000359596.7:c.14263A= ENSP00000352608.2:p.Asn4755=
ENST00000360985.7:c.14245A= ENSP00000354254.4:p.Asn4749=
NM_000540.2:c.14263A= , LRG_766t1:c.14263A= NP_000531.2:p.Asn4755=
NM_001042723.1:c.14248A= NP_001036188.1:p.Asn4750=
XM_006723317.1:c.14245A= XP_006723380.1:p.Asn4749=
XM_006723319.1:c.14230A= XP_006723382.1:p.Asn4744=
XM_011527204.1:c.14260A= XP_011525506.1:p.Asn4754=
XM_011527205.1:c.14176A= XP_011525507.1:p.Asn4726=
XM_006723317.2:c.14245A= XP_006723380.1:p.Asn4749=
XM_006723319.2:c.14230A= XP_006723382.1:p.Asn4744=
XM_011527205.2:c.14176A= XP_011525507.1:p.Asn4726=
NM_000540.3:c.14263A= MANE Select NP_000531.2:p.Asn4755=
NM_001042723.2:c.14248A= NP_001036188.1:p.Asn4750=