Canonical Allele Identifier: CA910794696

Gene: ROBO1

Linked Data

• dbSNP Id: rs1226815738
• MyVariant Identifiers: chr3:g.79603971G>A (hg19) ; chr3:g.79554821G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.79554821G>A , CM000665.2:g.79554821G>A	GRCh38
NC_000003.11:g.79603971G>A , CM000665.1:g.79603971G>A	GRCh37
NC_000003.10:g.79686661G>A	NCBI36
NG_011729.1:g.218089C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000464233.6:c.88+35003C>T MANE Select	ENSP00000420321.1:n.88+35003C>T
ENST00000464233.5:c.88+35003C>T	ENSP00000420321.1:n.88+35003C>T
ENST00000492990.1:c.89-21712C>T	ENSP00000419915.1:n.89-21712C>T
NM_002941.3:c.88+35003C>T	NP_002932.1:n.88+35003C>T
XM_011533976.1:c.88+35003C>T	XP_011532278.1:n.88+35003C>T
XM_011533977.1:c.88+35003C>T	XP_011532279.1:n.88+35003C>T
XM_011533978.1:c.88+35003C>T	XP_011532280.1:n.88+35003C>T
XM_011533979.1:c.88+35003C>T	XP_011532281.1:n.88+35003C>T
XM_011533980.1:c.88+35003C>T	XP_011532282.1:n.88+35003C>T
XM_011533977.2:c.88+35003C>T	XP_011532279.1:n.88+35003C>T
XM_017006982.1:c.88+35003C>T	XP_016862471.1:n.88+35003C>T
XM_017006984.1:c.88+35003C>T	XP_016862473.1:n.88+35003C>T
NM_002941.4:c.88+35003C>T MANE Select	NP_002932.1:n.88+35003C>T