Canonical Allele Identifier: CA353656883
Gene: ROBO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.78646147C>A , CM000665.2:g.78646147C>A GRCh38
NC_000003.11:g.78695297C>A , CM000665.1:g.78695297C>A GRCh37
NC_000003.10:g.78777987C>A NCBI36
NG_011729.1:g.1126763G>T

Transcript Alleles

HGVS Amino-acid Change
NM_002941.4:c.2882+1G>T MANE Select NP_002932.1:n.2882+1G>T
ENST00000464233.6:c.2882+1G>T MANE Select ENSP00000420321.1:n.2882+1G>T
NM_001145845.1:c.2747+1G>T NP_001139317.1:n.2747+1G>T
NM_001145845.2:c.2747+1G>T NP_001139317.1:n.2747+1G>T
NM_002941.3:c.2882+1G>T NP_002932.1:n.2882+1G>T
NM_133631.3:c.2747+1G>T NP_598334.2:n.2747+1G>T
NM_133631.4:c.2747+1G>T NP_598334.2:n.2747+1G>T
ENST00000436010.6:c.2522+1G>T ENSP00000406043.3:n.2522+1G>T
ENST00000464233.5:c.2882+1G>T ENSP00000420321.1:n.2882+1G>T
ENST00000467549.5:c.2747+1G>T ENSP00000417992.1:n.2747+1G>T
ENST00000495273.5:c.2747+1G>T ENSP00000420637.1:n.2747+1G>T
ENST00000498428.5:n.1779+1G>T
ENST00000618833.4:c.2747+1G>T ENSP00000477976.1:n.2747+1G>T
ENST00000618846.4:c.2504+1G>T ENSP00000482448.1:n.2504+1G>T
XM_006713276.2:c.2777+1G>T XP_006713339.1:n.2777+1G>T
XM_006713277.2:c.2774+1G>T XP_006713340.1:n.2774+1G>T
XM_006713277.3:c.2774+1G>T XP_006713340.1:n.2774+1G>T
XM_011533976.1:c.2891+1G>T XP_011532278.1:n.2891+1G>T
XM_011533977.1:c.2891+1G>T XP_011532279.1:n.2891+1G>T
XM_011533977.2:c.2891+1G>T XP_011532279.1:n.2891+1G>T
XM_011533978.1:c.2864+1G>T XP_011532280.1:n.2864+1G>T
XM_011533979.1:c.2891+1G>T XP_011532281.1:n.2891+1G>T
XM_011533980.1:c.2864+1G>T XP_011532282.1:n.2864+1G>T
XM_017006982.1:c.2807+1G>T XP_016862471.1:n.2807+1G>T
XM_017006983.2:c.2765+1G>T XP_016862472.1:n.2765+1G>T
XM_017006984.1:c.2882+1G>T XP_016862473.1:n.2882+1G>T
XM_017006985.1:c.2534+1G>T XP_016862474.1:n.2534+1G>T