Canonical Allele Identifier: CA2584900061
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38499858_38499859insGGCCCCGGCCGCCCCCCCCACCCCCCCC , CM000681.2:g.38499858_38499859insGGCCCCGGCCGCCCCCCCCACCCCCCCC GRCh38
NC_000019.9:g.38990498_38990499insGGCCCCGGCCGCCCCCCCCACCCCCCCC , CM000681.1:g.38990498_38990499insGGCCCCGGCCGCCCCCCCCACCCCCCCC GRCh37
NC_000019.8:g.43682338_43682339insGGCCCCGGCCGCCCCCCCCACCCCCCCC NCBI36
NG_008866.1:g.71159_71160insGGCCCCGGCCGCCCCCCCCACCCCCCCC , LRG_766:g.71159_71160insGGCCCCGGCCGCCCCCCCCACCCCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC ENSP00000471601.2:n.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCC...
ENST00000359596.8:c.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC MANE Select ENSP00000352608.2:n.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCC...
ENST00000355481.8:c.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC ENSP00000347667.3:n.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCC...
ENST00000359596.7:c.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC ENSP00000352608.2:n.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCC...
ENST00000360985.7:c.7211+37_7211+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC ENSP00000354254.4:n.7211+37_7211+38insGGCCCCGGCCGCCCCCCCCACCC...
ENST00000594335.5:c.666+37_666+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC
NM_000540.2:c.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC , LRG_766t1:c.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC NP_000531.2:n.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC
NM_001042723.1:c.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC NP_001036188.1:n.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCC...
XM_006723317.1:c.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC XP_006723380.1:n.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCC...
XM_006723319.1:c.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC XP_006723382.1:n.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCC...
XM_011527204.1:c.7211+37_7211+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC XP_011525506.1:n.7211+37_7211+38insGGCCCCGGCCGCCCCCCCCACCCCCC...
XM_011527205.1:c.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC XP_011525507.1:n.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCC...
XM_006723317.2:c.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC XP_006723380.1:n.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCC...
XM_006723319.2:c.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC XP_006723382.1:n.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCC...
XM_011527205.2:c.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC XP_011525507.1:n.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCC...
XR_001753735.1:n.7297+37_7297+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC
NM_000540.3:c.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC MANE Select NP_000531.2:n.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC
NM_001042723.2:c.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCCCC NP_001036188.1:n.7214+37_7214+38insGGCCCCGGCCGCCCCCCCCACCCCCC...