Canonical Allele Identifier: CA2535513663
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48342536del , CM000675.2:g.48342536del GRCh38
NC_000013.10:g.48916672del , CM000675.1:g.48916672del GRCh37
NC_000013.9:g.47814673del NCBI36
NG_009009.1:g.43790del , LRG_517:g.43790del

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.265-63del MANE Select ENSP00000267163.4:n.265-63del
ENST00000650461.1:c.265-63del ENSP00000497193.1:n.265-63del
ENST00000267163.4:c.265-63del ENSP00000267163.4:n.265-63del
ENST00000467505.5:c.138-17481del ENSP00000434702.1:n.138-17481del
ENST00000525036.1:n.427-63del
NM_000321.2:c.265-63del , LRG_517t1:c.265-63del NP_000312.2:n.265-63del
XM_011535171.1:c.4-63del XP_011533473.1:n.4-63del
XM_011535171.2:c.4-63del XP_011533473.1:n.4-63del
NM_000321.3:c.265-63del MANE Select NP_000312.2:n.265-63del