Canonical Allele Identifier: CA2335059636
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38512329G= , CM000681.2:g.38512329G= GRCh38
NC_000019.9:g.39002969G= , CM000681.1:g.39002969G= GRCh37
NC_000019.8:g.43694809G= NCBI36
NG_008866.1:g.83630G= , LRG_766:g.83630G=

Transcript Alleles

HGVS Amino-acid change
ENST00000599547.6:c.9257G= ENSP00000471601.2:n.9257G=
ENST00000359596.8:c.9318G= MANE Select ENSP00000352608.2:p.Met3106=
ENST00000355481.8:c.9318G= ENSP00000347667.3:p.Met3106=
ENST00000359596.7:c.9318G= ENSP00000352608.2:p.Met3106=
ENST00000360985.7:c.9315G= ENSP00000354254.4:p.Met3105=
ENST00000594335.5:c.2720G=
ENST00000599547.5:c.125G=
NM_000540.2:c.9318G= , LRG_766t1:c.9318G= NP_000531.2:p.Met3106=
NM_001042723.1:c.9318G= NP_001036188.1:p.Met3106=
XM_006723317.1:c.9318G= XP_006723380.1:p.Met3106=
XM_006723319.1:c.9318G= XP_006723382.1:p.Met3106=
XM_011527204.1:c.9315G= XP_011525506.1:p.Met3105=
XM_011527205.1:c.9318G= XP_011525507.1:p.Met3106=
XM_006723317.2:c.9318G= XP_006723380.1:p.Met3106=
XM_006723319.2:c.9318G= XP_006723382.1:p.Met3106=
XM_011527205.2:c.9318G= XP_011525507.1:p.Met3106=
XR_001753735.1:n.9351G=
NM_000540.3:c.9318G= MANE Select NP_000531.2:p.Met3106=
NM_001042723.2:c.9318G= NP_001036188.1:p.Met3106=