Canonical Allele Identifier: CA2335054825
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502913G= , CM000681.2:g.38502913G= GRCh38
NC_000019.9:g.38993553G= , CM000681.1:g.38993553G= GRCh37
NC_000019.8:g.43685393G= NCBI36
NG_008866.1:g.74214G= , LRG_766:g.74214G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7869G= ENSP00000471601.2:p.Leu2623=
ENST00000359596.8:c.7869G= MANE Select ENSP00000352608.2:p.Leu2623=
ENST00000355481.8:c.7869G= ENSP00000347667.3:p.Leu2623=
ENST00000359596.7:c.7869G= ENSP00000352608.2:p.Leu2623=
ENST00000360985.7:c.7866G= ENSP00000354254.4:p.Leu2622=
ENST00000594335.5:c.1321G=
NM_000540.2:c.7869G= , LRG_766t1:c.7869G= NP_000531.2:p.Leu2623=
NM_001042723.1:c.7869G= NP_001036188.1:p.Leu2623=
XM_006723317.1:c.7869G= XP_006723380.1:p.Leu2623=
XM_006723319.1:c.7869G= XP_006723382.1:p.Leu2623=
XM_011527204.1:c.7866G= XP_011525506.1:p.Leu2622=
XM_011527205.1:c.7869G= XP_011525507.1:p.Leu2623=
XM_006723317.2:c.7869G= XP_006723380.1:p.Leu2623=
XM_006723319.2:c.7869G= XP_006723382.1:p.Leu2623=
XM_011527205.2:c.7869G= XP_011525507.1:p.Leu2623=
XR_001753735.1:n.7952G=
NM_000540.3:c.7869G= MANE Select NP_000531.2:p.Leu2623=
NM_001042723.2:c.7869G= NP_001036188.1:p.Leu2623=