Canonical Allele Identifier: CA670417731
Gene: SLIT1 HGNC NCBI
ARHGAP19-SLIT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97171981T>A , CM000672.2:g.97171981T>A GRCh38
NC_000010.10:g.98931738T>A , CM000672.1:g.98931738T>A GRCh37
NC_000010.9:g.98921728T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266058.9:c.198-7091A>T (SLIT1) MANE Select ENSP00000266058.4:n.198-7091A>T
ENST00000266058.8:c.198-7091A>T (SLIT1) ENSP00000266058.4:n.198-7091A>T
ENST00000314867.9:c.147-7091A>T (SLIT1) ENSP00000315005.5:n.147-7091A>T
ENST00000371041.3:c.198-7091A>T (SLIT1) ENSP00000360080.3:n.198-7091A>T
ENST00000371070.8:c.198-7091A>T (SLIT1) ENSP00000360109.4:n.198-7091A>T
ENST00000456008.2:n.377-7091A>T (SLIT1)
ENST00000479633.2:c.1475-7091A>T (ARHGAP19-SLIT1) ENSP00000473567.1:n.1475-7091A>T
NM_003061.2:c.198-7091A>T (SLIT1) NP_003052.2:n.198-7091A>T
NR_037909.1:n.1521-7091A>T (ARHGAP19-SLIT1)
NM_003061.3:c.198-7091A>T (SLIT1) MANE Select NP_003052.2:n.198-7091A>T
Search 100 bp 5'
Search 100 bp 3'