Canonical Allele Identifier: CA405680961
Community Standard Title: NM_000540.3(RYR1):c.13904A>G (p.Glu4635Gly)
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38572176A>G , CM000681.2:g.38572176A>G GRCh38
NC_000019.9:g.39062816A>G , CM000681.1:g.39062816A>G GRCh37
NC_000019.8:g.43754656A>G NCBI36
NG_008866.1:g.143477A>G , LRG_766:g.143477A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000540.3:c.13904A>G MANE Select NP_000531.2:p.Glu4635Gly
ENST00000359596.8:c.13904A>G MANE Select ENSP00000352608.2:p.Glu4635Gly
NM_000540.2:c.13904A>G , LRG_766t1:c.13904A>G NP_000531.2:p.Glu4635Gly
NM_001042723.1:c.13889A>G NP_001036188.1:p.Glu4630Gly
NM_001042723.2:c.13889A>G NP_001036188.1:p.Glu4630Gly
ENST00000355481.8:c.13889A>G ENSP00000347667.3:p.Glu4630Gly
ENST00000359596.7:c.13904A>G ENSP00000352608.2:p.Glu4635Gly
ENST00000360985.7:c.13886A>G ENSP00000354254.4:p.Glu4629Gly
ENST00000593677.1:c.364A>G
ENST00000593677.2:c.840A>G
ENST00000688602.1:c.2237A>G
ENST00000689936.1:c.2209A>G
XM_006723317.1:c.13886A>G XP_006723380.1:p.Glu4629Gly
XM_006723317.2:c.13886A>G XP_006723380.1:p.Glu4629Gly
XM_006723319.1:c.13871A>G XP_006723382.1:p.Glu4624Gly
XM_006723319.2:c.13871A>G XP_006723382.1:p.Glu4624Gly
XM_011527204.1:c.13901A>G XP_011525506.1:p.Glu4634Gly
XM_011527205.1:c.13817A>G XP_011525507.1:p.Glu4606Gly
XM_011527205.2:c.13817A>G XP_011525507.1:p.Glu4606Gly