Canonical Allele Identifier: CA2335074539
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38543818G= , CM000681.2:g.38543818G= GRCh38
NC_000019.9:g.39034458G= , CM000681.1:g.39034458G= GRCh37
NC_000019.8:g.43726298G= NCBI36
NG_008866.1:g.115119G= , LRG_766:g.115119G=

Transcript Alleles

HGVS Amino-acid change
ENST00000688602.1:c.365G=
ENST00000689936.1:c.347G=
ENST00000359596.8:c.11955G= MANE Select ENSP00000352608.2:p.Trp3985=
ENST00000355481.8:c.11940G= ENSP00000347667.3:p.Trp3980=
ENST00000359596.7:c.11955G= ENSP00000352608.2:p.Trp3985=
ENST00000360985.7:c.11937G= ENSP00000354254.4:p.Trp3979=
ENST00000593322.1:c.564G=
ENST00000594335.5:c.5324G=
NM_000540.2:c.11955G= , LRG_766t1:c.11955G= NP_000531.2:p.Trp3985=
NM_001042723.1:c.11940G= NP_001036188.1:p.Trp3980=
XM_006723317.1:c.11937G= XP_006723380.1:p.Trp3979=
XM_006723319.1:c.11922G= XP_006723382.1:p.Trp3974=
XM_011527204.1:c.11952G= XP_011525506.1:p.Trp3984=
XM_011527205.1:c.11955G= XP_011525507.1:p.Trp3985=
XM_006723317.2:c.11937G= XP_006723380.1:p.Trp3979=
XM_006723319.2:c.11922G= XP_006723382.1:p.Trp3974=
XM_011527205.2:c.11955G= XP_011525507.1:p.Trp3985=
NM_000540.3:c.11955G= MANE Select NP_000531.2:p.Trp3985=
NM_001042723.2:c.11940G= NP_001036188.1:p.Trp3980=