Canonical Allele Identifier: CA11476908

Gene: ROBO1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.78627255T>C , CM000665.2:g.78627255T>C	GRCh38
NC_000003.11:g.78676405T>C , CM000665.1:g.78676405T>C	GRCh37
NC_000003.10:g.78759095T>C	NCBI36
NG_011729.1:g.1145655A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464233.6:c.3875+66A>G MANE Select	ENSP00000420321.1:n.3875+66A>G
ENST00000436010.6:c.3515+66A>G	ENSP00000406043.3:n.3515+66A>G
ENST00000464233.5:c.3875+66A>G	ENSP00000420321.1:n.3875+66A>G
ENST00000467549.5:c.3575+66A>G	ENSP00000417992.1:n.3575+66A>G
ENST00000495273.5:c.3740+66A>G	ENSP00000420637.1:n.3740+66A>G
ENST00000498428.5:n.2772+66A>G
ENST00000618833.4:c.3740+66A>G	ENSP00000477976.1:n.3740+66A>G
ENST00000618846.4:c.3497+66A>G	ENSP00000482448.1:n.3497+66A>G
NM_001145845.1:c.3575+66A>G	NP_001139317.1:n.3575+66A>G
NM_002941.3:c.3875+66A>G	NP_002932.1:n.3875+66A>G
NM_133631.3:c.3740+66A>G	NP_598334.2:n.3740+66A>G
XM_006713276.2:c.3770+66A>G	XP_006713339.1:n.3770+66A>G
XM_006713277.2:c.3767+66A>G	XP_006713340.1:n.3767+66A>G
XM_011533976.1:c.3884+66A>G	XP_011532278.1:n.3884+66A>G
XM_011533977.1:c.3884+66A>G	XP_011532279.1:n.3884+66A>G
XM_011533978.1:c.3857+66A>G	XP_011532280.1:n.3857+66A>G
XM_011533979.1:c.3719+66A>G	XP_011532281.1:n.3719+66A>G
XM_011533980.1:c.3692+66A>G	XP_011532282.1:n.3692+66A>G
XM_006713277.3:c.3767+66A>G	XP_006713340.1:n.3767+66A>G
XM_011533977.2:c.3884+66A>G	XP_011532279.1:n.3884+66A>G
XM_017006982.1:c.3800+66A>G	XP_016862471.1:n.3800+66A>G
XM_017006983.2:c.3758+66A>G	XP_016862472.1:n.3758+66A>G
XM_017006984.1:c.3710+66A>G	XP_016862473.1:n.3710+66A>G
XM_017006985.1:c.3527+66A>G	XP_016862474.1:n.3527+66A>G
NM_002941.4:c.3875+66A>G MANE Select	NP_002932.1:n.3875+66A>G
NM_001145845.2:c.3575+66A>G	NP_001139317.1:n.3575+66A>G
NM_133631.4:c.3740+66A>G	NP_598334.2:n.3740+66A>G