Canonical Allele Identifier: CA2575413241
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48304105del , CM000675.2:g.48304105del GRCh38
NC_000013.10:g.48878241del , CM000675.1:g.48878241del GRCh37
NC_000013.9:g.47776242del NCBI36
NG_009009.1:g.5359del , LRG_517:g.5359del

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.137+56del MANE Select ENSP00000267163.4:n.137+56del
ENST00000646097.1:c.137+56del ENSP00000496556.1:n.137+56del
ENST00000650461.1:c.137+56del ENSP00000497193.1:n.137+56del
ENST00000267163.4:c.137+56del ENSP00000267163.4:n.137+56del
ENST00000467505.5:c.137+56del ENSP00000434702.1:n.137+56del
ENST00000525036.1:n.299+56del
NM_000321.2:c.137+56del , LRG_517t1:c.137+56del NP_000312.2:n.137+56del
NM_000321.3:c.137+56del MANE Select NP_000312.2:n.137+56del