Canonical Allele Identifier: CA507354319
Gene: RYR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.39002900A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38512260A>C , CM000681.2:g.38512260A>C GRCh38
NC_000019.9:g.39002900A>C , CM000681.1:g.39002900A>C GRCh37
NC_000019.8:g.43694740A>C NCBI36
NG_008866.1:g.83561A>C , LRG_766:g.83561A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000599547.6:c.9188A>C ENSP00000471601.2:n.9188A>C
ENST00000359596.8:c.9249A>C MANE Select ENSP00000352608.2:p.Ser3083=
ENST00000355481.8:c.9249A>C ENSP00000347667.3:p.Ser3083=
ENST00000359596.7:c.9249A>C ENSP00000352608.2:p.Ser3083=
ENST00000360985.7:c.9246A>C ENSP00000354254.4:p.Ser3082=
ENST00000594335.5:c.2651A>C
ENST00000599547.5:c.56A>C
NM_000540.2:c.9249A>C , LRG_766t1:c.9249A>C NP_000531.2:p.Ser3083=
NM_001042723.1:c.9249A>C NP_001036188.1:p.Ser3083=
XM_006723317.1:c.9249A>C XP_006723380.1:p.Ser3083=
XM_006723319.1:c.9249A>C XP_006723382.1:p.Ser3083=
XM_011527204.1:c.9246A>C XP_011525506.1:p.Ser3082=
XM_011527205.1:c.9249A>C XP_011525507.1:p.Ser3083=
XM_006723317.2:c.9249A>C XP_006723380.1:p.Ser3083=
XM_006723319.2:c.9249A>C XP_006723382.1:p.Ser3083=
XM_011527205.2:c.9249A>C XP_011525507.1:p.Ser3083=
XR_001753735.1:n.9282A>C
NM_000540.3:c.9249A>C MANE Select NP_000531.2:p.Ser3083=
NM_001042723.2:c.9249A>C NP_001036188.1:p.Ser3083=