Canonical Allele Identifier: CA645571610
Gene: RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48459690_48459691insTA , CM000675.2:g.48459690_48459691insTA GRCh38
NC_000013.10:g.49033826_49033827insTA , CM000675.1:g.49033826_49033827insTA GRCh37
NC_000013.9:g.47931827_47931828insTA NCBI36
NG_009009.1:g.160944_160945insTA , LRG_517:g.160944_160945insTA

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1963_1964insTA MANE Select ENSP00000267163.4:p.Tyr655LeufsTer4
ENST00000643064.1:c.194+78247_194+78248insTA
ENST00000650461.1:c.1963_1964insTA ENSP00000497193.1:p.Tyr655LeufsTer4
ENST00000267163.4:c.1963_1964insTA ENSP00000267163.4:p.Tyr655LeufsTer4
NM_000321.2:c.1963_1964insTA , LRG_517t1:c.1963_1964insTA NP_000312.2:p.Tyr655LeufsTer4
XM_011535171.1:c.1702_1703insTA XP_011533473.1:p.Tyr568LeufsTer4
XM_011535171.2:c.1702_1703insTA XP_011533473.1:p.Tyr568LeufsTer4
NM_000321.3:c.1963_1964insTA MANE Select NP_000312.2:p.Tyr655LeufsTer4