Canonical Allele Identifier: CA2799116822

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48303762_48303763insCCTCA , CM000675.2:g.48303762_48303763insCCTCA	GRCh38
NC_000013.10:g.48877898_48877899insCCTCA , CM000675.1:g.48877898_48877899insCCTCA	GRCh37
NC_000013.9:g.47775899_47775900insCCTCA	NCBI36
NG_009009.1:g.5016_5017insCCTCA , LRG_517:g.5016_5017insCCTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.-151_-150insCCTCA MANE Select	ENSP00000267163.4:n.-151_-150insCCTCA
ENST00000646097.1:c.-151_-150insCCTCA	ENSP00000496556.1:n.-151_-150insCCTCA
ENST00000650461.1:c.-151_-150insCCTCA	ENSP00000497193.1:n.-151_-150insCCTCA
ENST00000525036.1:n.12_13insCCTCA
NM_000321.2:c.-151_-150insCCTCA , LRG_517t1:c.-151_-150insCCTCA	NP_000312.2:n.-151_-150insCCTCA
NM_000321.3:c.-151_-150insCCTCA MANE Select	NP_000312.2:n.-151_-150insCCTCA