Canonical Allele Identifier: CA2089972259

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48348632_48348636delinsATTTC , CM000675.2:g.48348632_48348636delinsATTTC	GRCh38
NC_000013.10:g.48922768_48922772delinsATTTC , CM000675.1:g.48922768_48922772delinsATTTC	GRCh37
NC_000013.9:g.47820769_47820773delinsATTTC	NCBI36
NG_009009.1:g.49886_49890delinsATTTC , LRG_517:g.49886_49890delinsATTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.540-324_540-320delinsATTTC MANE Select	ENSP00000267163.4:n.540-324_540-320delinsATTTC
ENST00000650461.1:c.540-324_540-320delinsATTTC	ENSP00000497193.1:n.540-324_540-320delinsATTTC
ENST00000267163.4:c.540-324_540-320delinsATTTC	ENSP00000267163.4:n.540-324_540-320delinsATTTC
ENST00000467505.5:c.138-11385_138-11381delinsATTTC	ENSP00000434702.1:n.138-11385_138-11381delinsATTTC
ENST00000525036.1:n.702-324_702-320delinsATTTC
NM_000321.2:c.540-324_540-320delinsATTTC , LRG_517t1:c.540-324_540-320delinsATTTC	NP_000312.2:n.540-324_540-320delinsATTTC
XM_011535171.1:c.279-324_279-320delinsATTTC	XP_011533473.1:n.279-324_279-320delinsATTTC
XM_011535171.2:c.279-324_279-320delinsATTTC	XP_011533473.1:n.279-324_279-320delinsATTTC
NM_000321.3:c.540-324_540-320delinsATTTC MANE Select	NP_000312.2:n.540-324_540-320delinsATTTC