Canonical Allele Identifier: CA2335089005
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38573264G= , CM000681.2:g.38573264G= GRCh38
NC_000019.9:g.39063904G= , CM000681.1:g.39063904G= GRCh37
NC_000019.8:g.43755744G= NCBI36
NG_008866.1:g.144565G= , LRG_766:g.144565G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1022G=
ENST00000688602.1:c.2419G=
ENST00000689936.1:c.2391G=
ENST00000359596.8:c.14086G= MANE Select ENSP00000352608.2:p.Asp4696=
ENST00000355481.8:c.14071G= ENSP00000347667.3:p.Asp4691=
ENST00000359596.7:c.14086G= ENSP00000352608.2:p.Asp4696=
ENST00000360985.7:c.14068G= ENSP00000354254.4:p.Asp4690=
NM_000540.2:c.14086G= , LRG_766t1:c.14086G= NP_000531.2:p.Asp4696=
NM_001042723.1:c.14071G= NP_001036188.1:p.Asp4691=
XM_006723317.1:c.14068G= XP_006723380.1:p.Asp4690=
XM_006723319.1:c.14053G= XP_006723382.1:p.Asp4685=
XM_011527204.1:c.14083G= XP_011525506.1:p.Asp4695=
XM_011527205.1:c.13999G= XP_011525507.1:p.Asp4667=
XM_006723317.2:c.14068G= XP_006723380.1:p.Asp4690=
XM_006723319.2:c.14053G= XP_006723382.1:p.Asp4685=
XM_011527205.2:c.13999G= XP_011525507.1:p.Asp4667=
NM_000540.3:c.14086G= MANE Select NP_000531.2:p.Asp4696=
NM_001042723.2:c.14071G= NP_001036188.1:p.Asp4691=