Canonical Allele Identifier: CA2089972386

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48348848_48348849delinsAT , CM000675.2:g.48348848_48348849delinsAT	GRCh38
NC_000013.10:g.48922984_48922985delinsAT , CM000675.1:g.48922984_48922985delinsAT	GRCh37
NC_000013.9:g.47820985_47820986delinsAT	NCBI36
NG_009009.1:g.50102_50103delinsAT , LRG_517:g.50102_50103delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.540-108_540-107delinsAT MANE Select	ENSP00000267163.4:n.540-108_540-107delinsAT
ENST00000650461.1:c.540-108_540-107delinsAT	ENSP00000497193.1:n.540-108_540-107delinsAT
ENST00000267163.4:c.540-108_540-107delinsAT	ENSP00000267163.4:n.540-108_540-107delinsAT
ENST00000467505.5:c.138-11169_138-11168delinsAT	ENSP00000434702.1:n.138-11169_138-11168delinsAT
ENST00000525036.1:n.702-108_702-107delinsAT
NM_000321.2:c.540-108_540-107delinsAT , LRG_517t1:c.540-108_540-107delinsAT	NP_000312.2:n.540-108_540-107delinsAT
XM_011535171.1:c.279-108_279-107delinsAT	XP_011533473.1:n.279-108_279-107delinsAT
XM_011535171.2:c.279-108_279-107delinsAT	XP_011533473.1:n.279-108_279-107delinsAT
NM_000321.3:c.540-108_540-107delinsAT MANE Select	NP_000312.2:n.540-108_540-107delinsAT