Canonical Allele Identifier: CA2695218621
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48459696_48459708delinsT , CM000675.2:g.48459696_48459708delinsT GRCh38
NC_000013.10:g.49033832_49033844delinsT , CM000675.1:g.49033832_49033844delinsT GRCh37
NC_000013.9:g.47931833_47931845delinsT NCBI36
NG_009009.1:g.160950_160962delinsT , LRG_517:g.160950_160962delinsT

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1969_1981delinsT MANE Select ENSP00000267163.4:p.Leu657_Arg661delinsTr...
ENST00000643064.1:c.194+78253_194+78265delinsT
ENST00000650461.1:c.1969_1981delinsT ENSP00000497193.1:p.Leu657_Arg661delinsTr...
ENST00000267163.4:c.1969_1981delinsT ENSP00000267163.4:p.Leu657_Arg661delinsTr...
NM_000321.2:c.1969_1981delinsT , LRG_517t1:c.1969_1981delinsT NP_000312.2:p.Leu657_Arg661delinsTrp
XM_011535171.1:c.1708_1720delinsT XP_011533473.1:p.Leu570_Arg574delinsTrp
XM_011535171.2:c.1708_1720delinsT XP_011533473.1:p.Leu570_Arg574delinsTrp
NM_000321.3:c.1969_1981delinsT MANE Select NP_000312.2:p.Leu657_Arg661delinsTrp