Canonical Allele Identifier: CA13165917

Gene: SLIT1 ARHGAP19-SLIT1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97170635T>C , CM000672.2:g.97170635T>C	GRCh38
NC_000010.10:g.98930392T>C , CM000672.1:g.98930392T>C	GRCh37
NC_000010.9:g.98920382T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266058.9:c.198-5745A>G (SLIT1) MANE Select	ENSP00000266058.4:n.198-5745A>G
ENST00000266058.8:c.198-5745A>G (SLIT1)	ENSP00000266058.4:n.198-5745A>G
ENST00000314867.9:c.147-5745A>G (SLIT1)	ENSP00000315005.5:n.147-5745A>G
ENST00000371041.3:c.198-5745A>G (SLIT1)	ENSP00000360080.3:n.198-5745A>G
ENST00000371070.8:c.198-5745A>G (SLIT1)	ENSP00000360109.4:n.198-5745A>G
ENST00000456008.2:n.377-5745A>G (SLIT1)
ENST00000479633.2:c.1475-5745A>G (ARHGAP19-SLIT1)	ENSP00000473567.1:n.1475-5745A>G
NM_003061.2:c.198-5745A>G (SLIT1)	NP_003052.2:n.198-5745A>G
NR_037909.1:n.1521-5745A>G (ARHGAP19-SLIT1)
NM_003061.3:c.198-5745A>G (SLIT1) MANE Select	NP_003052.2:n.198-5745A>G