Canonical Allele Identifier: CA1599586820

Gene: SLIT3

Genomic Alleles

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

Transcript Alleles

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