Canonical Allele Identifier: CA507355117
Gene: RYR1 HGNC NCBI

Linked Data

dbSNP Id: rs1971581914
MyVariant Identifiers: chr19:g.39019149C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38528509C>A , CM000681.2:g.38528509C>A GRCh38
NC_000019.9:g.39019149C>A , CM000681.1:g.39019149C>A GRCh37
NC_000019.8:g.43710989C>A NCBI36
NG_008866.1:g.99810C>A , LRG_766:g.99810C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000599547.6:c.10877-90C>A ENSP00000471601.2:n.10877-90C>A
ENST00000359596.8:c.10938-90C>A MANE Select ENSP00000352608.2:n.10938-90C>A
ENST00000355481.8:c.10923-90C>A ENSP00000347667.3:n.10923-90C>A
ENST00000359596.7:c.10938-90C>A ENSP00000352608.2:n.10938-90C>A
ENST00000360985.7:c.10920-90C>A ENSP00000354254.4:n.10920-90C>A
ENST00000594335.5:c.4325-90C>A
ENST00000599547.5:c.1745-90C>A
ENST00000601514.5:c.219-90C>A ENSP00000472497.1:n.219-90C>A
NM_000540.2:c.10938-90C>A , LRG_766t1:c.10938-90C>A NP_000531.2:n.10938-90C>A
NM_001042723.1:c.10923-90C>A NP_001036188.1:n.10923-90C>A
XM_006723317.1:c.10938-90C>A XP_006723380.1:n.10938-90C>A
XM_006723319.1:c.10923-90C>A XP_006723382.1:n.10923-90C>A
XM_011527204.1:c.10935-90C>A XP_011525506.1:n.10935-90C>A
XM_011527205.1:c.10938-90C>A XP_011525507.1:n.10938-90C>A
XM_006723317.2:c.10938-90C>A XP_006723380.1:n.10938-90C>A
XM_006723319.2:c.10923-90C>A XP_006723382.1:n.10923-90C>A
XM_011527205.2:c.10938-90C>A XP_011525507.1:n.10938-90C>A
XR_001753936.1:n.47G>T
NM_000540.3:c.10938-90C>A MANE Select NP_000531.2:n.10938-90C>A
NM_001042723.2:c.10923-90C>A NP_001036188.1:n.10923-90C>A