Canonical Allele Identifier: CA6344195

Gene: ROBO3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.124879223T>C , CM000673.2:g.124879223T>C	GRCh38
NC_000011.9:g.124749119T>C , CM000673.1:g.124749119T>C	GRCh37
NC_000011.8:g.124254329T>C	NCBI36
NG_016214.1:g.18815T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397801.6:c.3567T>C MANE Select	ENSP00000380903.1:p.Ser1189=
ENST00000397801.5:c.3567T>C	ENSP00000380903.1:p.Ser1189=
ENST00000524971.1:n.466T>C
ENST00000525304.5:n.387T>C
ENST00000525448.5:n.1329T>C
ENST00000525482.5:n.836T>C
ENST00000527196.5:n.1128T>C
ENST00000527245.5:n.2445T>C
ENST00000528144.5:n.622T>C
ENST00000528820.5:n.503T>C
ENST00000529658.5:n.1462T>C
ENST00000531075.5:n.275T>C
ENST00000538940.5:c.3501T>C	ENSP00000441797.1:p.Ser1167=
ENST00000543966.5:c.-145T>C	ENSP00000438799.1:n.-145T>C
NM_022370.3:c.3567T>C	NP_071765.2:p.Ser1189=
XM_011542953.1:c.4539T>C	XP_011541255.1:p.Ser1513=
XM_017018122.1:c.3501T>C	XP_016873611.1:p.Ser1167=
NM_022370.4:c.3567T>C MANE Select	NP_071765.2:p.Ser1189=
NM_001370356.1:c.714T>C	NP_001357285.1:p.Ser238=
NM_001370357.1:c.714T>C	NP_001357286.1:p.Ser238=
NM_001370358.1:c.714T>C	NP_001357287.1:p.Ser238=
NM_001370359.1:c.714T>C	NP_001357288.1:p.Ser238=
NM_001370361.1:c.714T>C	NP_001357290.1:p.Ser238=
NM_001370364.1:c.519T>C	NP_001357293.1:p.Ser173=
NM_001370366.1:c.519T>C	NP_001357295.1:p.Ser173=
NR_163409.1:n.715T>C
NR_163410.1:n.806T>C
NR_163411.1:n.958T>C
NR_163412.1:n.1001T>C
NR_163413.1:n.531T>C
NR_163414.1:n.782T>C
NR_163415.1:n.336T>C