Canonical Allele Identifier: CA10638195
Gene: ROBO3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.124878089T>G , CM000673.2:g.124878089T>G GRCh38
NC_000011.9:g.124747985T>G , CM000673.1:g.124747985T>G GRCh37
NC_000011.8:g.124253195T>G NCBI36
NG_016214.1:g.17681T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000397801.6:c.3139T>G MANE Select ENSP00000380903.1:p.Trp1047Gly
ENST00000397801.5:c.3139T>G ENSP00000380903.1:p.Trp1047Gly
ENST00000525448.5:n.901T>G
ENST00000525482.5:n.408T>G
ENST00000526551.5:n.315-209T>G
ENST00000527196.5:n.700T>G
ENST00000527245.5:n.1624T>G
ENST00000528144.5:n.375+431T>G
ENST00000528820.5:n.256+431T>G
ENST00000529658.5:n.1034T>G
ENST00000531075.5:n.241+431T>G
ENST00000534598.5:n.725T>G
ENST00000538940.5:c.3073T>G ENSP00000441797.1:p.Trp1025Gly
ENST00000543966.5:c.-434T>G ENSP00000438799.1:n.-434T>G
NM_022370.3:c.3139T>G NP_071765.2:p.Trp1047Gly
XM_011542953.1:c.4111T>G XP_011541255.1:p.Trp1371Gly
XM_017018122.1:c.3073T>G XP_016873611.1:p.Trp1025Gly
NM_022370.4:c.3139T>G MANE Select NP_071765.2:p.Trp1047Gly
NM_001370356.1:c.286T>G NP_001357285.1:p.Trp96Gly
NM_001370357.1:c.286T>G NP_001357286.1:p.Trp96Gly
NM_001370358.1:c.286T>G NP_001357287.1:p.Trp96Gly
NM_001370359.1:c.286T>G NP_001357288.1:p.Trp96Gly
NM_001370361.1:c.286T>G NP_001357290.1:p.Trp96Gly
NM_001370364.1:c.134-209T>G NP_001357293.1:n.134-209T>G
NM_001370366.1:c.134-209T>G NP_001357295.1:n.134-209T>G
NR_163409.1:n.639T>G
NR_163410.1:n.421-209T>G
NR_163411.1:n.530T>G
NR_163412.1:n.573T>G
NR_163413.1:n.284+431T>G
NR_163414.1:n.397-209T>G
NR_163415.1:n.302+431T>G