Canonical Allele Identifier: CA2335088994
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38573242C= , CM000681.2:g.38573242C= GRCh38
NC_000019.9:g.39063882C= , CM000681.1:g.39063882C= GRCh37
NC_000019.8:g.43755722C= NCBI36
NG_008866.1:g.144543C= , LRG_766:g.144543C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1000C=
ENST00000688602.1:c.2397C=
ENST00000689936.1:c.2369C=
ENST00000359596.8:c.14064C= MANE Select ENSP00000352608.2:p.Tyr4688=
ENST00000355481.8:c.14049C= ENSP00000347667.3:p.Tyr4683=
ENST00000359596.7:c.14064C= ENSP00000352608.2:p.Tyr4688=
ENST00000360985.7:c.14046C= ENSP00000354254.4:p.Tyr4682=
NM_000540.2:c.14064C= , LRG_766t1:c.14064C= NP_000531.2:p.Tyr4688=
NM_001042723.1:c.14049C= NP_001036188.1:p.Tyr4683=
XM_006723317.1:c.14046C= XP_006723380.1:p.Tyr4682=
XM_006723319.1:c.14031C= XP_006723382.1:p.Tyr4677=
XM_011527204.1:c.14061C= XP_011525506.1:p.Tyr4687=
XM_011527205.1:c.13977C= XP_011525507.1:p.Tyr4659=
XM_006723317.2:c.14046C= XP_006723380.1:p.Tyr4682=
XM_006723319.2:c.14031C= XP_006723382.1:p.Tyr4677=
XM_011527205.2:c.13977C= XP_011525507.1:p.Tyr4659=
NM_000540.3:c.14064C= MANE Select NP_000531.2:p.Tyr4688=
NM_001042723.2:c.14049C= NP_001036188.1:p.Tyr4683=