Canonical Allele Identifier: CA9845400
Gene: RBL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.37056247C>T , CM000682.2:g.37056247C>T GRCh38
NC_000020.10:g.35684650C>T , CM000682.1:g.35684650C>T GRCh37
NC_000020.9:g.35118064C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000373664.8:c.1262G>A MANE Select ENSP00000362768.3:p.Arg421His
ENST00000344359.7:c.1262G>A ENSP00000343646.3:p.Arg421His
ENST00000373664.7:c.1262G>A ENSP00000362768.3:p.Arg421His
ENST00000525052.1:c.676G>A
NM_002895.3:c.1262G>A NP_002886.2:p.Arg421His
NM_183404.2:c.1262G>A NP_899662.1:p.Arg421His
XM_006723842.1:c.746G>A XP_006723905.1:p.Arg249His
XM_011528955.1:c.1262G>A XP_011527257.1:p.Arg421His
XM_011528956.1:c.1025G>A XP_011527258.1:p.Arg342His
XM_011528957.1:c.950G>A XP_011527259.1:p.Arg317His
XM_011528958.1:c.1262G>A XP_011527260.1:p.Arg421His
XM_011528959.1:c.-20G>A XP_011527261.1:n.-20G>A
NM_001323281.1:c.-20G>A NP_001310210.1:n.-20G>A
NM_001323282.1:c.-20G>A NP_001310211.1:n.-20G>A
NM_002895.4:c.1262G>A NP_002886.2:p.Arg421His
NM_183404.3:c.1262G>A NP_899662.1:p.Arg421His
XM_006723842.3:c.746G>A XP_006723905.1:p.Arg249His
XM_017027992.1:c.950G>A XP_016883481.1:p.Arg317His
XM_024451956.1:c.1373G>A XP_024307724.1:p.Arg458His
XM_024451957.1:c.1373G>A XP_024307725.1:p.Arg458His
XM_024451958.1:c.1373G>A XP_024307726.1:p.Arg458His
NM_001323281.2:c.-20G>A NP_001310210.1:n.-20G>A
NM_001323282.2:c.-20G>A NP_001310211.1:n.-20G>A
NM_002895.5:c.1262G>A MANE Select NP_002886.2:p.Arg421His
NM_183404.4:c.1262G>A NP_899662.1:p.Arg421His