Canonical Allele Identifier: CA2089972087

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48381148_48381152delinsCCTTT , CM000675.2:g.48381148_48381152delinsCCTTT	GRCh38
NC_000013.10:g.48955284_48955288delinsCCTTT , CM000675.1:g.48955284_48955288delinsCCTTT	GRCh37
NC_000013.9:g.47853285_47853289delinsCCTTT	NCBI36
NG_009009.1:g.82402_82406delinsCCTTT , LRG_517:g.82402_82406delinsCCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.1499-99_1499-95delinsCCTTT MANE Select	ENSP00000267163.4:n.1499-99_1499-95delinsCCTTT
ENST00000650461.1:c.1499-99_1499-95delinsCCTTT	ENSP00000497193.1:n.1499-99_1499-95delinsCCTTT
ENST00000267163.4:c.1499-99_1499-95delinsCCTTT	ENSP00000267163.4:n.1499-99_1499-95delinsCCTTT
NM_000321.2:c.1499-99_1499-95delinsCCTTT , LRG_517t1:c.1499-99_1499-95delinsCCTTT	NP_000312.2:n.1499-99_1499-95delinsCCTTT
XM_011535171.1:c.1238-99_1238-95delinsCCTTT	XP_011533473.1:n.1238-99_1238-95delinsCCTTT
XM_011535171.2:c.1238-99_1238-95delinsCCTTT	XP_011533473.1:n.1238-99_1238-95delinsCCTTT
NM_000321.3:c.1499-99_1499-95delinsCCTTT MANE Select	NP_000312.2:n.1499-99_1499-95delinsCCTTT