Canonical Allele Identifier: CA1377689464
Gene: ROBO1 HGNC NCBI

Linked Data

dbSNP Id: rs1942638134

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.79554710G>C , CM000665.2:g.79554710G>C GRCh38
NC_000003.11:g.79603860G>C , CM000665.1:g.79603860G>C GRCh37
NC_000003.10:g.79686550G>C NCBI36
NG_011729.1:g.218200C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000464233.6:c.88+35114C>G MANE Select ENSP00000420321.1:n.88+35114C>G
ENST00000464233.5:c.88+35114C>G ENSP00000420321.1:n.88+35114C>G
ENST00000492990.1:c.89-21601C>G ENSP00000419915.1:n.89-21601C>G
NM_002941.3:c.88+35114C>G NP_002932.1:n.88+35114C>G
XM_011533976.1:c.88+35114C>G XP_011532278.1:n.88+35114C>G
XM_011533977.1:c.88+35114C>G XP_011532279.1:n.88+35114C>G
XM_011533978.1:c.88+35114C>G XP_011532280.1:n.88+35114C>G
XM_011533979.1:c.88+35114C>G XP_011532281.1:n.88+35114C>G
XM_011533980.1:c.88+35114C>G XP_011532282.1:n.88+35114C>G
XM_011533977.2:c.88+35114C>G XP_011532279.1:n.88+35114C>G
XM_017006982.1:c.88+35114C>G XP_016862471.1:n.88+35114C>G
XM_017006984.1:c.88+35114C>G XP_016862473.1:n.88+35114C>G
NM_002941.4:c.88+35114C>G MANE Select NP_002932.1:n.88+35114C>G