Canonical Allele Identifier: CA6344372

Gene: ROBO3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.124880546C>T , CM000673.2:g.124880546C>T	GRCh38
NC_000011.9:g.124750442C>T , CM000673.1:g.124750442C>T	GRCh37
NC_000011.8:g.124255652C>T	NCBI36
NG_016214.1:g.20138C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397801.6:c.4087C>T MANE Select	ENSP00000380903.1:p.Arg1363Trp
ENST00000397801.5:c.4087C>T	ENSP00000380903.1:p.Arg1363Trp
ENST00000525304.5:n.907C>T
ENST00000525448.5:n.1849C>T
ENST00000525482.5:n.1356C>T
ENST00000527196.5:n.1648C>T
ENST00000527245.5:n.2965C>T
ENST00000529658.5:n.1982C>T
ENST00000538940.5:c.4021C>T	ENSP00000441797.1:p.Arg1341Trp
ENST00000543966.5:c.376C>T	ENSP00000438799.1:p.Arg126Trp
NM_022370.3:c.4087C>T	NP_071765.2:p.Arg1363Trp
XM_011542953.1:c.5059C>T	XP_011541255.1:p.Arg1687Trp
XM_017018122.1:c.4021C>T	XP_016873611.1:p.Arg1341Trp
NM_022370.4:c.4087C>T MANE Select	NP_071765.2:p.Arg1363Trp
NM_001370356.1:c.1234C>T	NP_001357285.1:p.Arg412Trp
NM_001370357.1:c.1234C>T	NP_001357286.1:p.Arg412Trp
NM_001370358.1:c.1234C>T	NP_001357287.1:p.Arg412Trp
NM_001370359.1:c.1234C>T	NP_001357288.1:p.Arg412Trp
NM_001370361.1:c.1234C>T	NP_001357290.1:p.Arg412Trp
NM_001370364.1:c.1039C>T	NP_001357293.1:p.Arg347Trp
NM_001370366.1:c.1039C>T	NP_001357295.1:p.Arg347Trp
NR_163409.1:n.1235C>T
NR_163410.1:n.1326C>T
NR_163411.1:n.1478C>T
NR_163412.1:n.1521C>T
NR_163413.1:n.1051C>T
NR_163414.1:n.1302C>T
NR_163415.1:n.856C>T