Canonical Allele Identifier: CA2089970825

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48380023_48380025delinsCTT , CM000675.2:g.48380023_48380025delinsCTT	GRCh38
NC_000013.10:g.48954159_48954161delinsCTT , CM000675.1:g.48954159_48954161delinsCTT	GRCh37
NC_000013.9:g.47852160_47852162delinsCTT	NCBI36
NG_009009.1:g.81277_81279delinsCTT , LRG_517:g.81277_81279delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.1390-30_1390-28delinsCTT MANE Select	ENSP00000267163.4:n.1390-30_1390-28delinsCTT
ENST00000650461.1:c.1390-30_1390-28delinsCTT	ENSP00000497193.1:n.1390-30_1390-28delinsCTT
ENST00000267163.4:c.1390-30_1390-28delinsCTT	ENSP00000267163.4:n.1390-30_1390-28delinsCTT
NM_000321.2:c.1390-30_1390-28delinsCTT , LRG_517t1:c.1390-30_1390-28delinsCTT	NP_000312.2:n.1390-30_1390-28delinsCTT
XM_011535171.1:c.1129-30_1129-28delinsCTT	XP_011533473.1:n.1129-30_1129-28delinsCTT
XM_011535171.2:c.1129-30_1129-28delinsCTT	XP_011533473.1:n.1129-30_1129-28delinsCTT
NM_000321.3:c.1390-30_1390-28delinsCTT MANE Select	NP_000312.2:n.1390-30_1390-28delinsCTT