Canonical Allele Identifier: CA054848
Community Standard Title: NM_000540.3(RYR1):c.10824+8G>A
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38527792G>A , CM000681.2:g.38527792G>A GRCh38
NC_000019.9:g.39018432G>A , CM000681.1:g.39018432G>A GRCh37
NC_000019.8:g.43710272G>A NCBI36
NG_008866.1:g.99093G>A , LRG_766:g.99093G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000540.3:c.10824+8G>A MANE Select NP_000531.2:n.10824+8G>A
ENST00000359596.8:c.10824+8G>A MANE Select ENSP00000352608.2:n.10824+8G>A
NM_000540.2:c.10824+8G>A , LRG_766t1:c.10824+8G>A NP_000531.2:n.10824+8G>A
NM_001042723.1:c.10809+8G>A NP_001036188.1:n.10809+8G>A
NM_001042723.2:c.10809+8G>A NP_001036188.1:n.10809+8G>A
ENST00000355481.8:c.10809+8G>A ENSP00000347667.3:n.10809+8G>A
ENST00000359596.7:c.10824+8G>A ENSP00000352608.2:n.10824+8G>A
ENST00000360985.7:c.10806+8G>A ENSP00000354254.4:n.10806+8G>A
ENST00000594335.5:c.4211+8G>A
ENST00000599547.5:c.1631+8G>A
ENST00000599547.6:c.10763+8G>A ENSP00000471601.2:n.10763+8G>A
XM_006723317.1:c.10824+8G>A XP_006723380.1:n.10824+8G>A
XM_006723317.2:c.10824+8G>A XP_006723380.1:n.10824+8G>A
XM_006723319.1:c.10809+8G>A XP_006723382.1:n.10809+8G>A
XM_006723319.2:c.10809+8G>A XP_006723382.1:n.10809+8G>A
XM_011527204.1:c.10821+8G>A XP_011525506.1:n.10821+8G>A
XM_011527205.1:c.10824+8G>A XP_011525507.1:n.10824+8G>A
XM_011527205.2:c.10824+8G>A XP_011525507.1:n.10824+8G>A
XR_001753936.1:n.236-17C>T