Canonical Allele Identifier: CA2695218211
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303926_48303936del , CM000675.2:g.48303926_48303936del GRCh38
NC_000013.10:g.48878062_48878072del , CM000675.1:g.48878062_48878072del GRCh37
NC_000013.9:g.47776063_47776073del NCBI36
NG_009009.1:g.5180_5190del , LRG_517:g.5180_5190del

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.14_24del MANE Select ENSP00000267163.4:p.Thr5AsnfsTer22
ENST00000646097.1:c.14_24del ENSP00000496556.1:p.Thr5AsnfsTer22
ENST00000650461.1:c.14_24del ENSP00000497193.1:p.Thr5AsnfsTer22
ENST00000267163.4:c.14_24del ENSP00000267163.4:p.Thr5AsnfsTer22
ENST00000467505.5:c.14_24del ENSP00000434702.1:p.Thr5AsnfsTer22
ENST00000525036.1:n.176_186del
NM_000321.2:c.14_24del , LRG_517t1:c.14_24del NP_000312.2:p.Thr5AsnfsTer22
NM_000321.3:c.14_24del MANE Select NP_000312.2:p.Thr5AsnfsTer22