Canonical Allele Identifier: CA2695218217
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303967del , CM000675.2:g.48303967del GRCh38
NC_000013.10:g.48878103del , CM000675.1:g.48878103del GRCh37
NC_000013.9:g.47776104del NCBI36
NG_009009.1:g.5221del , LRG_517:g.5221del

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.55del MANE Select ENSP00000267163.4:p.Glu19AsnfsTer?
ENST00000646097.1:c.55del ENSP00000496556.1:p.Glu19AsnfsTer?
ENST00000650461.1:c.55del ENSP00000497193.1:p.Glu19AsnfsTer?
ENST00000267163.4:c.55del ENSP00000267163.4:p.Glu19AsnfsTer?
ENST00000467505.5:c.55del ENSP00000434702.1:p.Glu19AsnfsTer?
ENST00000525036.1:n.217del
NM_000321.2:c.55del , LRG_517t1:c.55del NP_000312.2:p.Glu19AsnfsTer?
NM_000321.3:c.55del MANE Select NP_000312.2:p.Glu19AsnfsTer?