Canonical Allele Identifier: CA405691108
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38455667G>T , CM000681.2:g.38455667G>T GRCh38
NC_000019.9:g.38946307G>T , CM000681.1:g.38946307G>T GRCh37
NC_000019.8:g.43638147G>T NCBI36
NG_008866.1:g.26968G>T , LRG_766:g.26968G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.1707G>T ENSP00000471601.2:p.Glu569Asp
ENST00000359596.8:c.1707G>T MANE Select ENSP00000352608.2:p.Glu569Asp
ENST00000355481.8:c.1707G>T ENSP00000347667.3:p.Glu569Asp
ENST00000359596.7:c.1707G>T ENSP00000352608.2:p.Glu569Asp
ENST00000360985.7:c.1707G>T ENSP00000354254.4:p.Glu569Asp
NM_000540.2:c.1707G>T , LRG_766t1:c.1707G>T NP_000531.2:p.Glu569Asp
NM_001042723.1:c.1707G>T NP_001036188.1:p.Glu569Asp
XM_006723317.1:c.1707G>T XP_006723380.1:p.Glu569Asp
XM_006723319.1:c.1707G>T XP_006723382.1:p.Glu569Asp
XM_011527204.1:c.1704G>T XP_011525506.1:p.Glu568Asp
XM_011527205.1:c.1707G>T XP_011525507.1:p.Glu569Asp
XM_006723317.2:c.1707G>T XP_006723380.1:p.Glu569Asp
XM_006723319.2:c.1707G>T XP_006723382.1:p.Glu569Asp
XM_011527205.2:c.1707G>T XP_011525507.1:p.Glu569Asp
XR_001753735.1:n.1790G>T
NM_000540.3:c.1707G>T MANE Select NP_000531.2:p.Glu569Asp
NM_001042723.2:c.1707G>T NP_001036188.1:p.Glu569Asp