Canonical Allele Identifier: CA507356027
Gene: RYR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.39062760C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38572120C>A , CM000681.2:g.38572120C>A GRCh38
NC_000019.9:g.39062760C>A , CM000681.1:g.39062760C>A GRCh37
NC_000019.8:g.43754600C>A NCBI36
NG_008866.1:g.143421C>A , LRG_766:g.143421C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.784C>A
ENST00000688602.1:c.2181C>A
ENST00000689936.1:c.2153C>A
ENST00000359596.8:c.13848C>A MANE Select ENSP00000352608.2:p.Ala4616=
ENST00000355481.8:c.13833C>A ENSP00000347667.3:p.Ala4611=
ENST00000359596.7:c.13848C>A ENSP00000352608.2:p.Ala4616=
ENST00000360985.7:c.13830C>A ENSP00000354254.4:p.Ala4610=
ENST00000593677.1:c.308C>A
NM_000540.2:c.13848C>A , LRG_766t1:c.13848C>A NP_000531.2:p.Ala4616=
NM_001042723.1:c.13833C>A NP_001036188.1:p.Ala4611=
XM_006723317.1:c.13830C>A XP_006723380.1:p.Ala4610=
XM_006723319.1:c.13815C>A XP_006723382.1:p.Ala4605=
XM_011527204.1:c.13845C>A XP_011525506.1:p.Ala4615=
XM_011527205.1:c.13761C>A XP_011525507.1:p.Ala4587=
XM_006723317.2:c.13830C>A XP_006723380.1:p.Ala4610=
XM_006723319.2:c.13815C>A XP_006723382.1:p.Ala4605=
XM_011527205.2:c.13761C>A XP_011525507.1:p.Ala4587=
NM_000540.3:c.13848C>A MANE Select NP_000531.2:p.Ala4616=
NM_001042723.2:c.13833C>A NP_001036188.1:p.Ala4611=