Canonical Allele Identifier: CA2090013968
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48452944_48452945delinsGA , CM000675.2:g.48452944_48452945delinsGA GRCh38
NC_000013.10:g.49027080_49027081delinsGA , CM000675.1:g.49027080_49027081delinsGA GRCh37
NC_000013.9:g.47925081_47925082delinsGA NCBI36
NG_009009.1:g.154198_154199delinsGA , LRG_517:g.154198_154199delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1696-49_1696-48delinsGA MANE Select ENSP00000267163.4:n.1696-49_1696-48delins...
ENST00000643064.1:c.194+71501_194+71502delinsGA
ENST00000650461.1:c.1696-49_1696-48delinsGA ENSP00000497193.1:n.1696-49_1696-48delins...
ENST00000267163.4:c.1696-49_1696-48delinsGA ENSP00000267163.4:n.1696-49_1696-48delins...
ENST00000480491.1:n.395-49_395-48delinsGA
NM_000321.2:c.1696-49_1696-48delinsGA , LRG_517t1:c.1696-49_1696-48delinsGA NP_000312.2:n.1696-49_1696-48delinsGA
XM_011535171.1:c.1435-49_1435-48delinsGA XP_011533473.1:n.1435-49_1435-48delinsGA
XM_011535171.2:c.1435-49_1435-48delinsGA XP_011533473.1:n.1435-49_1435-48delinsGA
NM_000321.3:c.1696-49_1696-48delinsGA MANE Select NP_000312.2:n.1696-49_1696-48delinsGA