Canonical Allele Identifier: CA6344131

Gene: ROBO3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.124878617T>A , CM000673.2:g.124878617T>A	GRCh38
NC_000011.9:g.124748513T>A , CM000673.1:g.124748513T>A	GRCh37
NC_000011.8:g.124253723T>A	NCBI36
NG_016214.1:g.18209T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397801.6:c.3354T>A MANE Select	ENSP00000380903.1:p.Pro1118=
ENST00000397801.5:c.3354T>A	ENSP00000380903.1:p.Pro1118=
ENST00000524971.1:n.253T>A
ENST00000525304.5:n.174T>A
ENST00000525448.5:n.1116T>A
ENST00000525482.5:n.623T>A
ENST00000526551.5:n.487T>A
ENST00000527196.5:n.915T>A
ENST00000527245.5:n.1839T>A
ENST00000528144.5:n.409T>A
ENST00000528820.5:n.290T>A
ENST00000529658.5:n.1249T>A
ENST00000531075.5:n.242-573T>A
ENST00000538940.5:c.3288T>A	ENSP00000441797.1:p.Pro1096=
ENST00000543966.5:c.-358T>A	ENSP00000438799.1:n.-358T>A
NM_022370.3:c.3354T>A	NP_071765.2:p.Pro1118=
XM_011542953.1:c.4326T>A	XP_011541255.1:p.Pro1442=
XM_017018122.1:c.3288T>A	XP_016873611.1:p.Pro1096=
NM_022370.4:c.3354T>A MANE Select	NP_071765.2:p.Pro1118=
NM_001370356.1:c.501T>A	NP_001357285.1:p.Pro167=
NM_001370357.1:c.501T>A	NP_001357286.1:p.Pro167=
NM_001370358.1:c.501T>A	NP_001357287.1:p.Pro167=
NM_001370359.1:c.501T>A	NP_001357288.1:p.Pro167=
NM_001370361.1:c.501T>A	NP_001357290.1:p.Pro167=
NM_001370364.1:c.306T>A	NP_001357293.1:p.Pro102=
NM_001370366.1:c.306T>A	NP_001357295.1:p.Pro102=
NR_163409.1:n.681+486T>A
NR_163410.1:n.593T>A
NR_163411.1:n.745T>A
NR_163412.1:n.788T>A
NR_163413.1:n.318T>A
NR_163414.1:n.569T>A
NR_163415.1:n.303-573T>A