Canonical Allele Identifier: CA1377254624
Gene: ROBO1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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