Canonical Allele Identifier: CA353679829
Gene: ROBO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.78746779A>T , CM000665.2:g.78746779A>T GRCh38
NC_000003.11:g.78795929A>T , CM000665.1:g.78795929A>T GRCh37
NC_000003.10:g.78878619A>T NCBI36
NG_011729.1:g.1026131T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000464233.6:c.621T>A MANE Select ENSP00000420321.1:p.Asp207Glu
ENST00000436010.6:c.264T>A ENSP00000406043.3:p.Asp88Glu
ENST00000464233.5:c.621T>A ENSP00000420321.1:p.Asp207Glu
ENST00000467549.5:c.504T>A ENSP00000417992.1:p.Asp168Glu
ENST00000495273.5:c.504T>A ENSP00000420637.1:p.Asp168Glu
ENST00000618833.4:c.504T>A ENSP00000477976.1:p.Asp168Glu
ENST00000618846.4:c.264T>A ENSP00000482448.1:p.Asp88Glu
NM_001145845.1:c.504T>A NP_001139317.1:p.Asp168Glu
NM_002941.3:c.621T>A NP_002932.1:p.Asp207Glu
NM_133631.3:c.504T>A NP_598334.2:p.Asp168Glu
XM_006713276.2:c.507T>A XP_006713339.1:p.Asp169Glu
XM_006713277.2:c.504T>A XP_006713340.1:p.Asp168Glu
XM_011533976.1:c.621T>A XP_011532278.1:p.Asp207Glu
XM_011533977.1:c.621T>A XP_011532279.1:p.Asp207Glu
XM_011533978.1:c.621T>A XP_011532280.1:p.Asp207Glu
XM_011533979.1:c.621T>A XP_011532281.1:p.Asp207Glu
XM_011533980.1:c.621T>A XP_011532282.1:p.Asp207Glu
XM_006713277.3:c.504T>A XP_006713340.1:p.Asp168Glu
XM_011533977.2:c.621T>A XP_011532279.1:p.Asp207Glu
XM_017006982.1:c.537T>A XP_016862471.1:p.Asp179Glu
XM_017006983.2:c.504T>A XP_016862472.1:p.Asp168Glu
XM_017006984.1:c.621T>A XP_016862473.1:p.Asp207Glu
XM_017006985.1:c.264T>A XP_016862474.1:p.Asp88Glu
NM_002941.4:c.621T>A MANE Select NP_002932.1:p.Asp207Glu
NM_001145845.2:c.504T>A NP_001139317.1:p.Asp168Glu
NM_133631.4:c.504T>A NP_598334.2:p.Asp168Glu