Canonical Allele Identifier: CA1443092319

Gene: SLIT2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.20619347C= , CM000666.2:g.20619347C=	GRCh38
NC_000004.11:g.20620970C= , CM000666.1:g.20620970C=	GRCh37
NC_000004.10:g.20230068C=	NCBI36
NG_047105.1:g.372423C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504154.6:c.*338C= MANE Select	ENSP00000422591.1:n.*338C=
ENST00000504154.5:c.*338C=	ENSP00000422591.1:n.*338C=
ENST00000512993.1:c.237-1057C=
ENST00000622093.4:c.*338C=	ENSP00000482129.1:n.*338C=
NM_001289135.1:c.*338C=	NP_001276064.1:n.*338C=
NM_001289135.2:c.*338C=	NP_001276064.1:n.*338C=
NM_001289136.1:c.*338C=	NP_001276065.1:n.*338C=
NM_001289136.2:c.*338C=	NP_001276065.1:n.*338C=
NM_004787.2:c.*338C=	NP_004778.1:n.*338C=
NM_004787.3:c.*338C=	NP_004778.1:n.*338C=
XM_005248211.2:c.*338C=	XP_005248268.1:n.*338C=
XM_006713986.2:c.*338C=	XP_006714049.1:n.*338C=
XM_011513909.1:c.*338C=	XP_011512211.1:n.*338C=
XM_011513910.1:c.*338C=	XP_011512212.1:n.*338C=
XM_005248211.3:c.*338C=	XP_005248268.1:n.*338C=
XM_006713986.3:c.*338C=	XP_006714049.1:n.*338C=
XM_011513909.2:c.*338C=	XP_011512211.1:n.*338C=
XM_011513910.2:c.*338C=	XP_011512212.2:n.*338C=
XM_017008845.1:c.*338C=	XP_016864334.1:n.*338C=
NM_004787.4:c.*338C= MANE Select	NP_004778.1:n.*338C=
NM_001289135.3:c.*338C=	NP_001276064.1:n.*338C=
NM_001289136.3:c.*338C=	NP_001276065.1:n.*338C=