Canonical Allele Identifier: CA2756943351
Gene: ROBO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.79555073C>A , CM000665.2:g.79555073C>A GRCh38
NC_000003.11:g.79604223C>A , CM000665.1:g.79604223C>A GRCh37
NC_000003.10:g.79686913C>A NCBI36
NG_011729.1:g.217837G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000464233.6:c.88+34751G>T MANE Select ENSP00000420321.1:n.88+34751G>T
ENST00000464233.5:c.88+34751G>T ENSP00000420321.1:n.88+34751G>T
ENST00000492990.1:c.89-21964G>T ENSP00000419915.1:n.89-21964G>T
NM_002941.3:c.88+34751G>T NP_002932.1:n.88+34751G>T
XM_011533976.1:c.88+34751G>T XP_011532278.1:n.88+34751G>T
XM_011533977.1:c.88+34751G>T XP_011532279.1:n.88+34751G>T
XM_011533978.1:c.88+34751G>T XP_011532280.1:n.88+34751G>T
XM_011533979.1:c.88+34751G>T XP_011532281.1:n.88+34751G>T
XM_011533980.1:c.88+34751G>T XP_011532282.1:n.88+34751G>T
XM_011533977.2:c.88+34751G>T XP_011532279.1:n.88+34751G>T
XM_017006982.1:c.88+34751G>T XP_016862471.1:n.88+34751G>T
XM_017006984.1:c.88+34751G>T XP_016862473.1:n.88+34751G>T
NM_002941.4:c.88+34751G>T MANE Select NP_002932.1:n.88+34751G>T