Canonical Allele Identifier: CA6344300
Gene: ROBO3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.124879826C>T , CM000673.2:g.124879826C>T GRCh38
NC_000011.9:g.124749722C>T , CM000673.1:g.124749722C>T GRCh37
NC_000011.8:g.124254932C>T NCBI36
NG_016214.1:g.19418C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000397801.6:c.3836C>T MANE Select ENSP00000380903.1:p.Ala1279Val
ENST00000397801.5:c.3836C>T ENSP00000380903.1:p.Ala1279Val
ENST00000524971.1:n.735C>T
ENST00000525304.5:n.656C>T
ENST00000525448.5:n.1598C>T
ENST00000525482.5:n.1105C>T
ENST00000527196.5:n.1397C>T
ENST00000527245.5:n.2714C>T
ENST00000528820.5:n.772C>T
ENST00000529658.5:n.1731C>T
ENST00000531075.5:n.544C>T
ENST00000538940.5:c.3770C>T ENSP00000441797.1:p.Ala1257Val
ENST00000543966.5:c.125C>T ENSP00000438799.1:p.Ala42Val
NM_022370.3:c.3836C>T NP_071765.2:p.Ala1279Val
XM_011542953.1:c.4808C>T XP_011541255.1:p.Ala1603Val
XM_017018122.1:c.3770C>T XP_016873611.1:p.Ala1257Val
NM_022370.4:c.3836C>T MANE Select NP_071765.2:p.Ala1279Val
NM_001370356.1:c.983C>T NP_001357285.1:p.Ala328Val
NM_001370357.1:c.983C>T NP_001357286.1:p.Ala328Val
NM_001370358.1:c.983C>T NP_001357287.1:p.Ala328Val
NM_001370359.1:c.983C>T NP_001357288.1:p.Ala328Val
NM_001370361.1:c.983C>T NP_001357290.1:p.Ala328Val
NM_001370364.1:c.788C>T NP_001357293.1:p.Ala263Val
NM_001370366.1:c.788C>T NP_001357295.1:p.Ala263Val
NR_163409.1:n.984C>T
NR_163410.1:n.1075C>T
NR_163411.1:n.1227C>T
NR_163412.1:n.1270C>T
NR_163413.1:n.800C>T
NR_163414.1:n.1051C>T
NR_163415.1:n.605C>T