Canonical Allele Identifier: CA645578638
Gene: RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48364961del , CM000675.2:g.48364961del GRCh38
NC_000013.10:g.48939097del , CM000675.1:g.48939097del GRCh37
NC_000013.9:g.47837098del NCBI36
NG_009009.1:g.66215del , LRG_517:g.66215del

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.929del MANE Select ENSP00000267163.4:p.Gly310AspfsTer22
ENST00000650461.1:c.929del ENSP00000497193.1:p.Gly310AspfsTer22
ENST00000267163.4:c.929del ENSP00000267163.4:p.Gly310AspfsTer22
NM_000321.2:c.929del , LRG_517t1:c.929del NP_000312.2:p.Gly310AspfsTer22
XM_011535171.1:c.668del XP_011533473.1:p.Gly223AspfsTer22
XM_011535171.2:c.668del XP_011533473.1:p.Gly223AspfsTer22
XR_002957522.1:n.138del
NM_000321.3:c.929del MANE Select NP_000312.2:p.Gly310AspfsTer22