Canonical Allele Identifier: CA6344323
Gene: ROBO3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.124879911C>T , CM000673.2:g.124879911C>T GRCh38
NC_000011.9:g.124749807C>T , CM000673.1:g.124749807C>T GRCh37
NC_000011.8:g.124255017C>T NCBI36
NG_016214.1:g.19503C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000397801.6:c.3921C>T MANE Select ENSP00000380903.1:p.Ala1307=
ENST00000397801.5:c.3921C>T ENSP00000380903.1:p.Ala1307=
ENST00000524971.1:n.820C>T
ENST00000525304.5:n.741C>T
ENST00000525448.5:n.1683C>T
ENST00000525482.5:n.1190C>T
ENST00000527196.5:n.1482C>T
ENST00000527245.5:n.2799C>T
ENST00000529658.5:n.1816C>T
ENST00000531075.5:n.629C>T
ENST00000538940.5:c.3855C>T ENSP00000441797.1:p.Ala1285=
ENST00000543966.5:c.210C>T ENSP00000438799.1:p.Ala70=
NM_022370.3:c.3921C>T NP_071765.2:p.Ala1307=
XM_011542953.1:c.4893C>T XP_011541255.1:p.Ala1631=
XM_017018122.1:c.3855C>T XP_016873611.1:p.Ala1285=
NM_022370.4:c.3921C>T MANE Select NP_071765.2:p.Ala1307=
NM_001370356.1:c.1068C>T NP_001357285.1:p.Ala356=
NM_001370357.1:c.1068C>T NP_001357286.1:p.Ala356=
NM_001370358.1:c.1068C>T NP_001357287.1:p.Ala356=
NM_001370359.1:c.1068C>T NP_001357288.1:p.Ala356=
NM_001370361.1:c.1068C>T NP_001357290.1:p.Ala356=
NM_001370364.1:c.873C>T NP_001357293.1:p.Ala291=
NM_001370366.1:c.873C>T NP_001357295.1:p.Ala291=
NR_163409.1:n.1069C>T
NR_163410.1:n.1160C>T
NR_163411.1:n.1312C>T
NR_163412.1:n.1355C>T
NR_163413.1:n.885C>T
NR_163414.1:n.1136C>T
NR_163415.1:n.690C>T