Canonical Allele Identifier: CA2335096106
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38587333T= , CM000681.2:g.38587333T= GRCh38
NC_000019.9:g.39077973T= , CM000681.1:g.39077973T= GRCh37
NC_000019.8:g.43769813T= NCBI36
NG_008866.1:g.158634T= , LRG_766:g.158634T=

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.1957+757T=
ENST00000688602.1:c.3363T=
ENST00000689936.1:c.3335T=
ENST00000692547.1:n.423T=
ENST00000359596.8:c.15030T= MANE Select ENSP00000352608.2:p.Tyr5010=
ENST00000355481.8:c.15015T= ENSP00000347667.3:p.Tyr5005=
ENST00000359596.7:c.15030T= ENSP00000352608.2:p.Tyr5010=
ENST00000360985.7:c.15012T= ENSP00000354254.4:p.Tyr5004=
NM_000540.2:c.15030T= , LRG_766t1:c.15030T= NP_000531.2:p.Tyr5010=
NM_001042723.1:c.15015T= NP_001036188.1:p.Tyr5005=
XM_006723317.1:c.15012T= XP_006723380.1:p.Tyr5004=
XM_006723319.1:c.14997T= XP_006723382.1:p.Tyr4999=
XM_011527204.1:c.15027T= XP_011525506.1:p.Tyr5009=
XM_011527205.1:c.14943T= XP_011525507.1:p.Tyr4981=
XM_006723317.2:c.15012T= XP_006723380.1:p.Tyr5004=
XM_006723319.2:c.14997T= XP_006723382.1:p.Tyr4999=
XM_011527205.2:c.14943T= XP_011525507.1:p.Tyr4981=
NM_000540.3:c.15030T= MANE Select NP_000531.2:p.Tyr5010=
NM_001042723.2:c.15015T= NP_001036188.1:p.Tyr5005=