Canonical Allele Identifier: CA1377689513

Gene: ROBO1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.79554822C= , CM000665.2:g.79554822C=	GRCh38
NC_000003.11:g.79603972C= , CM000665.1:g.79603972C=	GRCh37
NC_000003.10:g.79686662C=	NCBI36
NG_011729.1:g.218088G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000464233.6:c.88+35002G= MANE Select	ENSP00000420321.1:n.88+35002G=
ENST00000464233.5:c.88+35002G=	ENSP00000420321.1:n.88+35002G=
ENST00000492990.1:c.89-21713G=	ENSP00000419915.1:n.89-21713G=
NM_002941.3:c.88+35002G=	NP_002932.1:n.88+35002G=
XM_011533976.1:c.88+35002G=	XP_011532278.1:n.88+35002G=
XM_011533977.1:c.88+35002G=	XP_011532279.1:n.88+35002G=
XM_011533978.1:c.88+35002G=	XP_011532280.1:n.88+35002G=
XM_011533979.1:c.88+35002G=	XP_011532281.1:n.88+35002G=
XM_011533980.1:c.88+35002G=	XP_011532282.1:n.88+35002G=
XM_011533977.2:c.88+35002G=	XP_011532279.1:n.88+35002G=
XM_017006982.1:c.88+35002G=	XP_016862471.1:n.88+35002G=
XM_017006984.1:c.88+35002G=	XP_016862473.1:n.88+35002G=
NM_002941.4:c.88+35002G= MANE Select	NP_002932.1:n.88+35002G=