Canonical Allele Identifier: CA2089971109
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48380136_48380137delinsAT , CM000675.2:g.48380136_48380137delinsAT GRCh38
NC_000013.10:g.48954272_48954273delinsAT , CM000675.1:g.48954272_48954273delinsAT GRCh37
NC_000013.9:g.47852273_47852274delinsAT NCBI36
NG_009009.1:g.81390_81391delinsAT , LRG_517:g.81390_81391delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.1422-29_1422-28delinsAT MANE Select ENSP00000267163.4:n.1422-29_1422-28delinsAT
ENST00000650461.1:c.1422-29_1422-28delinsAT ENSP00000497193.1:n.1422-29_1422-28delinsAT
ENST00000267163.4:c.1422-29_1422-28delinsAT ENSP00000267163.4:n.1422-29_1422-28delinsAT
NM_000321.2:c.1422-29_1422-28delinsAT , LRG_517t1:c.1422-29_1422-28delinsAT NP_000312.2:n.1422-29_1422-28delinsAT
XM_011535171.1:c.1161-29_1161-28delinsAT XP_011533473.1:n.1161-29_1161-28delinsAT
XM_011535171.2:c.1161-29_1161-28delinsAT XP_011533473.1:n.1161-29_1161-28delinsAT
NM_000321.3:c.1422-29_1422-28delinsAT MANE Select NP_000312.2:n.1422-29_1422-28delinsAT