Canonical Allele Identifier: CA10637686
Gene: ROBO3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.124879486G>T , CM000673.2:g.124879486G>T GRCh38
NC_000011.9:g.124749382G>T , CM000673.1:g.124749382G>T GRCh37
NC_000011.8:g.124254592G>T NCBI36
NG_016214.1:g.19078G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000397801.6:c.3707G>T MANE Select ENSP00000380903.1:p.Gly1236Val
ENST00000397801.5:c.3707G>T ENSP00000380903.1:p.Gly1236Val
ENST00000524971.1:n.606G>T
ENST00000525304.5:n.527G>T
ENST00000525448.5:n.1469G>T
ENST00000525482.5:n.976G>T
ENST00000527196.5:n.1268G>T
ENST00000527245.5:n.2585G>T
ENST00000528820.5:n.643G>T
ENST00000529658.5:n.1602G>T
ENST00000531075.5:n.415G>T
ENST00000538940.5:c.3641G>T ENSP00000441797.1:p.Gly1214Val
ENST00000543966.5:c.-5G>T ENSP00000438799.1:n.-5G>T
NM_022370.3:c.3707G>T NP_071765.2:p.Gly1236Val
XM_011542953.1:c.4679G>T XP_011541255.1:p.Gly1560Val
XM_017018122.1:c.3641G>T XP_016873611.1:p.Gly1214Val
NM_022370.4:c.3707G>T MANE Select NP_071765.2:p.Gly1236Val
NM_001370356.1:c.854G>T NP_001357285.1:p.Gly285Val
NM_001370357.1:c.854G>T NP_001357286.1:p.Gly285Val
NM_001370358.1:c.854G>T NP_001357287.1:p.Gly285Val
NM_001370359.1:c.854G>T NP_001357288.1:p.Gly285Val
NM_001370361.1:c.854G>T NP_001357290.1:p.Gly285Val
NM_001370364.1:c.659G>T NP_001357293.1:p.Gly220Val
NM_001370366.1:c.659G>T NP_001357295.1:p.Gly220Val
NR_163409.1:n.855G>T
NR_163410.1:n.946G>T
NR_163411.1:n.1098G>T
NR_163412.1:n.1141G>T
NR_163413.1:n.671G>T
NR_163414.1:n.922G>T
NR_163415.1:n.476G>T