Canonical Allele Identifier: CA77693146

Gene: ROBO1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.78871694C>A , CM000665.2:g.78871694C>A	GRCh38
NC_000003.11:g.78920844C>A , CM000665.1:g.78920844C>A	GRCh37
NC_000003.10:g.79003534C>A	NCBI36
NG_011729.1:g.901216G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464233.6:c.499+66907G>T MANE Select	ENSP00000420321.1:n.499+66907G>T
ENST00000436010.6:c.142+66907G>T	ENSP00000406043.3:n.142+66907G>T
ENST00000464233.5:c.499+66907G>T	ENSP00000420321.1:n.499+66907G>T
ENST00000467549.5:c.382+66907G>T	ENSP00000417992.1:n.382+66907G>T
ENST00000495273.5:c.382+66907G>T	ENSP00000420637.1:n.382+66907G>T
ENST00000618833.4:c.382+66907G>T	ENSP00000477976.1:n.382+66907G>T
ENST00000618846.4:c.142+66907G>T	ENSP00000482448.1:n.142+66907G>T
NM_001145845.1:c.382+66907G>T	NP_001139317.1:n.382+66907G>T
NM_002941.3:c.499+66907G>T	NP_002932.1:n.499+66907G>T
NM_133631.3:c.382+66907G>T	NP_598334.2:n.382+66907G>T
XM_006713276.2:c.385+66907G>T	XP_006713339.1:n.385+66907G>T
XM_006713277.2:c.382+66907G>T	XP_006713340.1:n.382+66907G>T
XM_011533976.1:c.499+66907G>T	XP_011532278.1:n.499+66907G>T
XM_011533977.1:c.499+66907G>T	XP_011532279.1:n.499+66907G>T
XM_011533978.1:c.499+66907G>T	XP_011532280.1:n.499+66907G>T
XM_011533979.1:c.499+66907G>T	XP_011532281.1:n.499+66907G>T
XM_011533980.1:c.499+66907G>T	XP_011532282.1:n.499+66907G>T
XM_006713277.3:c.382+66907G>T	XP_006713340.1:n.382+66907G>T
XM_011533977.2:c.499+66907G>T	XP_011532279.1:n.499+66907G>T
XM_017006982.1:c.415+66907G>T	XP_016862471.1:n.415+66907G>T
XM_017006983.2:c.382+66907G>T	XP_016862472.1:n.382+66907G>T
XM_017006984.1:c.499+66907G>T	XP_016862473.1:n.499+66907G>T
XM_017006985.1:c.142+66907G>T	XP_016862474.1:n.142+66907G>T
NM_002941.4:c.499+66907G>T MANE Select	NP_002932.1:n.499+66907G>T
NM_001145845.2:c.382+66907G>T	NP_001139317.1:n.382+66907G>T
NM_133631.4:c.382+66907G>T	NP_598334.2:n.382+66907G>T