Canonical Allele Identifier: CA2335052923
Gene: RYR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38499764T= , CM000681.2:g.38499764T= GRCh38
NC_000019.9:g.38990404T= , CM000681.1:g.38990404T= GRCh37
NC_000019.8:g.43682244T= NCBI36
NG_008866.1:g.71065T= , LRG_766:g.71065T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7157T= ENSP00000471601.2:p.Ile2386=
ENST00000359596.8:c.7157T= MANE Select ENSP00000352608.2:p.Ile2386=
ENST00000355481.8:c.7157T= ENSP00000347667.3:p.Ile2386=
ENST00000359596.7:c.7157T= ENSP00000352608.2:p.Ile2386=
ENST00000360985.7:c.7154T= ENSP00000354254.4:p.Ile2385=
ENST00000594335.5:c.609T=
NM_000540.2:c.7157T= , LRG_766t1:c.7157T= NP_000531.2:p.Ile2386=
NM_001042723.1:c.7157T= NP_001036188.1:p.Ile2386=
XM_006723317.1:c.7157T= XP_006723380.1:p.Ile2386=
XM_006723319.1:c.7157T= XP_006723382.1:p.Ile2386=
XM_011527204.1:c.7154T= XP_011525506.1:p.Ile2385=
XM_011527205.1:c.7157T= XP_011525507.1:p.Ile2386=
XM_006723317.2:c.7157T= XP_006723380.1:p.Ile2386=
XM_006723319.2:c.7157T= XP_006723382.1:p.Ile2386=
XM_011527205.2:c.7157T= XP_011525507.1:p.Ile2386=
XR_001753735.1:n.7240T=
NM_000540.3:c.7157T= MANE Select NP_000531.2:p.Ile2386=
NM_001042723.2:c.7157T= NP_001036188.1:p.Ile2386=
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