Canonical Allele Identifier: CA2089970841
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48380036_48380037delinsTA , CM000675.2:g.48380036_48380037delinsTA GRCh38
NC_000013.10:g.48954172_48954173delinsTA , CM000675.1:g.48954172_48954173delinsTA GRCh37
NC_000013.9:g.47852173_47852174delinsTA NCBI36
NG_009009.1:g.81290_81291delinsTA , LRG_517:g.81290_81291delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1390-17_1390-16delinsTA MANE Select ENSP00000267163.4:n.1390-17_1390-16delinsTA
ENST00000650461.1:c.1390-17_1390-16delinsTA ENSP00000497193.1:n.1390-17_1390-16delinsTA
ENST00000267163.4:c.1390-17_1390-16delinsTA ENSP00000267163.4:n.1390-17_1390-16delinsTA
NM_000321.2:c.1390-17_1390-16delinsTA , LRG_517t1:c.1390-17_1390-16delinsTA NP_000312.2:n.1390-17_1390-16delinsTA
XM_011535171.1:c.1129-17_1129-16delinsTA XP_011533473.1:n.1129-17_1129-16delinsTA
XM_011535171.2:c.1129-17_1129-16delinsTA XP_011533473.1:n.1129-17_1129-16delinsTA
NM_000321.3:c.1390-17_1390-16delinsTA MANE Select NP_000312.2:n.1390-17_1390-16delinsTA