Canonical Allele Identifier: CA2584901128
Gene: RYR1 HGNC NCBI

Linked Data

gnomAD v4: 19-38502938-ATCC-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502941_38502943del , CM000681.2:g.38502941_38502943del GRCh38
NC_000019.9:g.38993581_38993583del , CM000681.1:g.38993581_38993583del GRCh37
NC_000019.8:g.43685421_43685423del NCBI36
NG_008866.1:g.74242_74244del , LRG_766:g.74242_74244del

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7897_7899del ENSP00000471601.2:p.Leu2633del
ENST00000359596.8:c.7897_7899del MANE Select ENSP00000352608.2:p.Leu2633del
ENST00000355481.8:c.7897_7899del ENSP00000347667.3:p.Leu2633del
ENST00000359596.7:c.7897_7899del ENSP00000352608.2:p.Leu2633del
ENST00000360985.7:c.7894_7896del ENSP00000354254.4:p.Leu2632del
ENST00000594335.5:c.1349_1351del
NM_000540.2:c.7897_7899del , LRG_766t1:c.7897_7899del NP_000531.2:p.Leu2633del
NM_001042723.1:c.7897_7899del NP_001036188.1:p.Leu2633del
XM_006723317.1:c.7897_7899del XP_006723380.1:p.Leu2633del
XM_006723319.1:c.7897_7899del XP_006723382.1:p.Leu2633del
XM_011527204.1:c.7894_7896del XP_011525506.1:p.Leu2632del
XM_011527205.1:c.7897_7899del XP_011525507.1:p.Leu2633del
XM_006723317.2:c.7897_7899del XP_006723380.1:p.Leu2633del
XM_006723319.2:c.7897_7899del XP_006723382.1:p.Leu2633del
XM_011527205.2:c.7897_7899del XP_011525507.1:p.Leu2633del
XR_001753735.1:n.7980_7982del
NM_000540.3:c.7897_7899del MANE Select NP_000531.2:p.Leu2633del
NM_001042723.2:c.7897_7899del NP_001036188.1:p.Leu2633del
Search 100 bp 5'
Search 100 bp 3'