Canonical Allele Identifier: CA2576771041
Gene: RYR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38499041_38499047del , CM000681.2:g.38499041_38499047del GRCh38
NC_000019.9:g.38989681_38989687del , CM000681.1:g.38989681_38989687del GRCh37
NC_000019.8:g.43681521_43681527del NCBI36
NG_008866.1:g.70342_70348del , LRG_766:g.70342_70348del

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.6892-67_6892-61del ENSP00000471601.2:n.6892-67_6892-61del
ENST00000359596.8:c.6892-67_6892-61del MANE Select ENSP00000352608.2:n.6892-67_6892-61del
ENST00000355481.8:c.6892-67_6892-61del ENSP00000347667.3:n.6892-67_6892-61del
ENST00000359596.7:c.6892-67_6892-61del ENSP00000352608.2:n.6892-67_6892-61del
ENST00000360985.7:c.6889-67_6889-61del ENSP00000354254.4:n.6889-67_6889-61del
ENST00000594335.5:c.344-67_344-61del
NM_000540.2:c.6892-67_6892-61del , LRG_766t1:c.6892-67_6892-61del NP_000531.2:n.6892-67_6892-61del
NM_001042723.1:c.6892-67_6892-61del NP_001036188.1:n.6892-67_6892-61del
XM_006723317.1:c.6892-67_6892-61del XP_006723380.1:n.6892-67_6892-61del
XM_006723319.1:c.6892-67_6892-61del XP_006723382.1:n.6892-67_6892-61del
XM_011527204.1:c.6889-67_6889-61del XP_011525506.1:n.6889-67_6889-61del
XM_011527205.1:c.6892-67_6892-61del XP_011525507.1:n.6892-67_6892-61del
XM_006723317.2:c.6892-67_6892-61del XP_006723380.1:n.6892-67_6892-61del
XM_006723319.2:c.6892-67_6892-61del XP_006723382.1:n.6892-67_6892-61del
XM_011527205.2:c.6892-67_6892-61del XP_011525507.1:n.6892-67_6892-61del
XR_001753735.1:n.6975-67_6975-61del
NM_000540.3:c.6892-67_6892-61del MANE Select NP_000531.2:n.6892-67_6892-61del
NM_001042723.2:c.6892-67_6892-61del NP_001036188.1:n.6892-67_6892-61del