Canonical Allele Identifier: CA1599586822
Gene: SLIT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.168768351G>C , CM000667.2:g.168768351G>C GRCh38
NC_000005.9:g.168195356G>C , CM000667.1:g.168195356G>C GRCh37
NC_000005.8:g.168127934G>C NCBI36
NG_033081.1:g.537778C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000519560.6:c.1459+4430C>G MANE Select ENSP00000430333.2:n.1459+4430C>G
ENST00000332966.8:c.1459+4430C>G ENSP00000332164.8:n.1459+4430C>G
ENST00000404867.7:c.1048+4430C>G ENSP00000384890.4:n.1048+4430C>G
ENST00000519486.5:n.3162+4430C>G
ENST00000519560.5:c.1459+4430C>G ENSP00000430333.1:n.1459+4430C>G
NM_001271946.1:c.1459+4430C>G NP_001258875.1:n.1459+4430C>G
NM_003062.3:c.1459+4430C>G NP_003053.1:n.1459+4430C>G
XM_017009779.1:c.1270+4430C>G XP_016865268.1:n.1270+4430C>G
NM_001271946.2:c.1459+4430C>G NP_001258875.2:n.1459+4430C>G
NM_003062.4:c.1459+4430C>G MANE Select NP_003053.2:n.1459+4430C>G