Canonical Allele Identifier: CA2335054550
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502769_38502771delinsAGG , CM000681.2:g.38502769_38502771delinsAGG GRCh38
NC_000019.9:g.38993409_38993411delinsAGG , CM000681.1:g.38993409_38993411delinsAGG GRCh37
NC_000019.8:g.43685249_43685251delinsAGG NCBI36
NG_008866.1:g.74070_74072delinsAGG , LRG_766:g.74070_74072delinsAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7835+42_7835+44delinsAGG ENSP00000471601.2:n.7835+42_7835+44delinsAGG
ENST00000359596.8:c.7835+42_7835+44delinsAGG MANE Select ENSP00000352608.2:n.7835+42_7835+44delinsAGG
ENST00000355481.8:c.7835+42_7835+44delinsAGG ENSP00000347667.3:n.7835+42_7835+44delinsAGG
ENST00000359596.7:c.7835+42_7835+44delinsAGG ENSP00000352608.2:n.7835+42_7835+44delinsAGG
ENST00000360985.7:c.7832+42_7832+44delinsAGG ENSP00000354254.4:n.7832+42_7832+44delinsAGG
ENST00000594335.5:c.1287+42_1287+44delinsAGG
NM_000540.2:c.7835+42_7835+44delinsAGG , LRG_766t1:c.7835+42_7835+44delinsAGG NP_000531.2:n.7835+42_7835+44delinsAGG
NM_001042723.1:c.7835+42_7835+44delinsAGG NP_001036188.1:n.7835+42_7835+44delinsAGG
XM_006723317.1:c.7835+42_7835+44delinsAGG XP_006723380.1:n.7835+42_7835+44delinsAGG
XM_006723319.1:c.7835+42_7835+44delinsAGG XP_006723382.1:n.7835+42_7835+44delinsAGG
XM_011527204.1:c.7832+42_7832+44delinsAGG XP_011525506.1:n.7832+42_7832+44delinsAGG
XM_011527205.1:c.7835+42_7835+44delinsAGG XP_011525507.1:n.7835+42_7835+44delinsAGG
XM_006723317.2:c.7835+42_7835+44delinsAGG XP_006723380.1:n.7835+42_7835+44delinsAGG
XM_006723319.2:c.7835+42_7835+44delinsAGG XP_006723382.1:n.7835+42_7835+44delinsAGG
XM_011527205.2:c.7835+42_7835+44delinsAGG XP_011525507.1:n.7835+42_7835+44delinsAGG
XR_001753735.1:n.7918+42_7918+44delinsAGG
NM_000540.3:c.7835+42_7835+44delinsAGG MANE Select NP_000531.2:n.7835+42_7835+44delinsAGG
NM_001042723.2:c.7835+42_7835+44delinsAGG NP_001036188.1:n.7835+42_7835+44delinsAGG