Canonical Allele Identifier: CA2335067452
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38528607C= , CM000681.2:g.38528607C= GRCh38
NC_000019.9:g.39019247C= , CM000681.1:g.39019247C= GRCh37
NC_000019.8:g.43711087C= NCBI36
NG_008866.1:g.99908C= , LRG_766:g.99908C=

Transcript Alleles

HGVS Amino-acid change
ENST00000599547.6:c.10885C= ENSP00000471601.2:n.10885C=
ENST00000359596.8:c.10946C= MANE Select ENSP00000352608.2:p.Ala3649=
ENST00000355481.8:c.10931C= ENSP00000347667.3:p.Ala3644=
ENST00000359596.7:c.10946C= ENSP00000352608.2:p.Ala3649=
ENST00000360985.7:c.10928C= ENSP00000354254.4:p.Ala3643=
ENST00000594335.5:c.4333C=
ENST00000599547.5:c.1753C=
ENST00000601514.5:c.227C= ENSP00000472497.1:p.Ala76=
NM_000540.2:c.10946C= , LRG_766t1:c.10946C= NP_000531.2:p.Ala3649=
NM_001042723.1:c.10931C= NP_001036188.1:p.Ala3644=
XM_006723317.1:c.10946C= XP_006723380.1:p.Ala3649=
XM_006723319.1:c.10931C= XP_006723382.1:p.Ala3644=
XM_011527204.1:c.10943C= XP_011525506.1:p.Ala3648=
XM_011527205.1:c.10946C= XP_011525507.1:p.Ala3649=
XM_006723317.2:c.10946C= XP_006723380.1:p.Ala3649=
XM_006723319.2:c.10931C= XP_006723382.1:p.Ala3644=
XM_011527205.2:c.10946C= XP_011525507.1:p.Ala3649=
NM_000540.3:c.10946C= MANE Select NP_000531.2:p.Ala3649=
NM_001042723.2:c.10931C= NP_001036188.1:p.Ala3644=