Canonical Allele Identifier: CA1443013731

Gene: SLIT2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.20493512C= , CM000666.2:g.20493512C=	GRCh38
NC_000004.11:g.20495135C= , CM000666.1:g.20495135C=	GRCh37
NC_000004.10:g.20104233C=	NCBI36
NG_047105.1:g.246588C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504154.6:c.914+1613C= MANE Select	ENSP00000422591.1:n.914+1613C=
ENST00000273739.9:c.926+1613C=	ENSP00000273739.5:n.926+1613C=
ENST00000503823.5:c.914+1613C=	ENSP00000427548.1:n.914+1613C=
ENST00000503837.5:c.926+1613C=	ENSP00000422261.1:n.926+1613C=
ENST00000504154.5:c.914+1613C=	ENSP00000422591.1:n.914+1613C=
ENST00000622093.4:c.668+1613C=	ENSP00000482129.1:n.668+1613C=
NM_001289135.1:c.926+1613C=	NP_001276064.1:n.926+1613C=
NM_001289135.2:c.926+1613C=	NP_001276064.1:n.926+1613C=
NM_001289136.1:c.914+1613C=	NP_001276065.1:n.914+1613C=
NM_001289136.2:c.914+1613C=	NP_001276065.1:n.914+1613C=
NM_004787.2:c.914+1613C=	NP_004778.1:n.914+1613C=
NM_004787.3:c.914+1613C=	NP_004778.1:n.914+1613C=
XM_005248211.2:c.926+1613C=	XP_005248268.1:n.926+1613C=
XM_006713986.2:c.926+1613C=	XP_006714049.1:n.926+1613C=
XM_011513909.1:c.824+1613C=	XP_011512211.1:n.824+1613C=
XM_005248211.3:c.926+1613C=	XP_005248268.1:n.926+1613C=
XM_006713986.3:c.926+1613C=	XP_006714049.1:n.926+1613C=
XM_011513909.2:c.824+1613C=	XP_011512211.1:n.824+1613C=
XM_017008845.1:c.812+1613C=	XP_016864334.1:n.812+1613C=
NM_004787.4:c.914+1613C= MANE Select	NP_004778.1:n.914+1613C=
NM_001289135.3:c.926+1613C=	NP_001276064.1:n.926+1613C=
NM_001289136.3:c.914+1613C=	NP_001276065.1:n.914+1613C=