Canonical Allele Identifier: CA6344102

Gene: ROBO3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.124878416G>A , CM000673.2:g.124878416G>A	GRCh38
NC_000011.9:g.124748312G>A , CM000673.1:g.124748312G>A	GRCh37
NC_000011.8:g.124253522G>A	NCBI36
NG_016214.1:g.18008G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397801.6:c.3300G>A MANE Select	ENSP00000380903.1:p.Pro1100=
ENST00000397801.5:c.3300G>A	ENSP00000380903.1:p.Pro1100=
ENST00000524971.1:n.52G>A
ENST00000525304.5:n.120G>A
ENST00000525448.5:n.1062G>A
ENST00000525482.5:n.569G>A
ENST00000526551.5:n.433G>A
ENST00000527196.5:n.861G>A
ENST00000527245.5:n.1785G>A
ENST00000528144.5:n.376-168G>A
ENST00000528820.5:n.257-168G>A
ENST00000529658.5:n.1195G>A
ENST00000531075.5:n.241+758G>A
ENST00000538940.5:c.3234G>A	ENSP00000441797.1:p.Pro1078=
ENST00000543966.5:c.-391-168G>A	ENSP00000438799.1:n.-391-168G>A
NM_022370.3:c.3300G>A	NP_071765.2:p.Pro1100=
XM_011542953.1:c.4272G>A	XP_011541255.1:p.Pro1424=
XM_017018122.1:c.3234G>A	XP_016873611.1:p.Pro1078=
NM_022370.4:c.3300G>A MANE Select	NP_071765.2:p.Pro1100=
NM_001370356.1:c.447G>A	NP_001357285.1:p.Pro149=
NM_001370357.1:c.447G>A	NP_001357286.1:p.Pro149=
NM_001370358.1:c.447G>A	NP_001357287.1:p.Pro149=
NM_001370359.1:c.447G>A	NP_001357288.1:p.Pro149=
NM_001370361.1:c.447G>A	NP_001357290.1:p.Pro149=
NM_001370364.1:c.252G>A	NP_001357293.1:p.Pro84=
NM_001370366.1:c.252G>A	NP_001357295.1:p.Pro84=
NR_163409.1:n.681+285G>A
NR_163410.1:n.539G>A
NR_163411.1:n.691G>A
NR_163412.1:n.734G>A
NR_163413.1:n.285-168G>A
NR_163414.1:n.515G>A
NR_163415.1:n.302+758G>A