Canonical Allele Identifier: CA1377689390
Gene: ROBO1 HGNC NCBI

Linked Data

dbSNP Id: rs1942632440

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.79554553_79554554insACA , CM000665.2:g.79554553_79554554insACA GRCh38
NC_000003.11:g.79603703_79603704insACA , CM000665.1:g.79603703_79603704insACA GRCh37
NC_000003.10:g.79686393_79686394insACA NCBI36
NG_011729.1:g.218356_218357insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000464233.6:c.88+35270_88+35271insTGT MANE Select ENSP00000420321.1:n.88+35270_88+35271insTGT
ENST00000464233.5:c.88+35270_88+35271insTGT ENSP00000420321.1:n.88+35270_88+35271insTGT
ENST00000492990.1:c.89-21445_89-21444insTGT ENSP00000419915.1:n.89-21445_89-21444insTGT
NM_002941.3:c.88+35270_88+35271insTGT NP_002932.1:n.88+35270_88+35271insTGT
XM_011533976.1:c.88+35270_88+35271insTGT XP_011532278.1:n.88+35270_88+35271insTGT
XM_011533977.1:c.88+35270_88+35271insTGT XP_011532279.1:n.88+35270_88+35271insTGT
XM_011533978.1:c.88+35270_88+35271insTGT XP_011532280.1:n.88+35270_88+35271insTGT
XM_011533979.1:c.88+35270_88+35271insTGT XP_011532281.1:n.88+35270_88+35271insTGT
XM_011533980.1:c.88+35270_88+35271insTGT XP_011532282.1:n.88+35270_88+35271insTGT
XM_011533977.2:c.88+35270_88+35271insTGT XP_011532279.1:n.88+35270_88+35271insTGT
XM_017006982.1:c.88+35270_88+35271insTGT XP_016862471.1:n.88+35270_88+35271insTGT
XM_017006984.1:c.88+35270_88+35271insTGT XP_016862473.1:n.88+35270_88+35271insTGT
NM_002941.4:c.88+35270_88+35271insTGT MANE Select NP_002932.1:n.88+35270_88+35271insTGT