Canonical Allele Identifier: CA2831039853
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48364923del , CM000675.2:g.48364923del GRCh38
NC_000013.10:g.48939059del , CM000675.1:g.48939059del GRCh37
NC_000013.9:g.47837060del NCBI36
NG_009009.1:g.66177del , LRG_517:g.66177del

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.891del MANE Select ENSP00000267163.4:p.Pro298LeufsTer3
ENST00000650461.1:c.891del ENSP00000497193.1:p.Pro298LeufsTer3
ENST00000267163.4:c.891del ENSP00000267163.4:p.Pro298LeufsTer3
NM_000321.2:c.891del , LRG_517t1:c.891del NP_000312.2:p.Pro298LeufsTer3
XM_011535171.1:c.630del XP_011533473.1:p.Pro211LeufsTer3
XM_011535171.2:c.630del XP_011533473.1:p.Pro211LeufsTer3
XR_002957522.1:n.175del
NM_000321.3:c.891del MANE Select NP_000312.2:p.Pro298LeufsTer3