Canonical Allele Identifier: CA2335088983
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38573217G= , CM000681.2:g.38573217G= GRCh38
NC_000019.9:g.39063857G= , CM000681.1:g.39063857G= GRCh37
NC_000019.8:g.43755697G= NCBI36
NG_008866.1:g.144518G= , LRG_766:g.144518G=

Transcript Alleles

HGVS Amino-acid change
ENST00000593677.2:c.975G=
ENST00000688602.1:c.2372G=
ENST00000689936.1:c.2344G=
ENST00000359596.8:c.14039G= MANE Select ENSP00000352608.2:p.Arg4680=
ENST00000355481.8:c.14024G= ENSP00000347667.3:p.Arg4675=
ENST00000359596.7:c.14039G= ENSP00000352608.2:p.Arg4680=
ENST00000360985.7:c.14021G= ENSP00000354254.4:p.Arg4674=
NM_000540.2:c.14039G= , LRG_766t1:c.14039G= NP_000531.2:p.Arg4680=
NM_001042723.1:c.14024G= NP_001036188.1:p.Arg4675=
XM_006723317.1:c.14021G= XP_006723380.1:p.Arg4674=
XM_006723319.1:c.14006G= XP_006723382.1:p.Arg4669=
XM_011527204.1:c.14036G= XP_011525506.1:p.Arg4679=
XM_011527205.1:c.13952G= XP_011525507.1:p.Arg4651=
XM_006723317.2:c.14021G= XP_006723380.1:p.Arg4674=
XM_006723319.2:c.14006G= XP_006723382.1:p.Arg4669=
XM_011527205.2:c.13952G= XP_011525507.1:p.Arg4651=
NM_000540.3:c.14039G= MANE Select NP_000531.2:p.Arg4680=
NM_001042723.2:c.14024G= NP_001036188.1:p.Arg4675=