Canonical Allele Identifier: CA2799116855
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303987_48303988del , CM000675.2:g.48303987_48303988del GRCh38
NC_000013.10:g.48878123_48878124del , CM000675.1:g.48878123_48878124del GRCh37
NC_000013.9:g.47776124_47776125del NCBI36
NG_009009.1:g.5241_5242del , LRG_517:g.5241_5242del

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.75_76del MANE Select ENSP00000267163.4:p.Pro26AlafsTer4
ENST00000646097.1:c.75_76del ENSP00000496556.1:p.Pro26AlafsTer4
ENST00000650461.1:c.75_76del ENSP00000497193.1:p.Pro26AlafsTer4
ENST00000267163.4:c.75_76del ENSP00000267163.4:p.Pro26AlafsTer4
ENST00000467505.5:c.75_76del ENSP00000434702.1:p.Pro26AlafsTer4
ENST00000525036.1:n.237_238del
NM_000321.2:c.75_76del , LRG_517t1:c.75_76del NP_000312.2:p.Pro26AlafsTer4
NM_000321.3:c.75_76del MANE Select NP_000312.2:p.Pro26AlafsTer4