Canonical Allele Identifier: CA2760665791

Gene: SLIT2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.20619180_20619182del , CM000666.2:g.20619180_20619182del	GRCh38
NC_000004.11:g.20620803_20620805del , CM000666.1:g.20620803_20620805del	GRCh37
NC_000004.10:g.20229901_20229903del	NCBI36
NG_047105.1:g.372256_372258del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504154.6:c.*171_*173del MANE Select	ENSP00000422591.1:n.*171_*173del
ENST00000273739.9:c.*171_*173del	ENSP00000273739.5:n.*171_*173del
ENST00000503837.5:c.4749_4751del	ENSP00000422261.1:n.4749_4751del
ENST00000504154.5:c.*171_*173del	ENSP00000422591.1:n.*171_*173del
ENST00000512993.1:c.237-1224_237-1222del
ENST00000622093.4:c.*171_*173del	ENSP00000482129.1:n.*171_*173del
NM_001289135.1:c.*171_*173del	NP_001276064.1:n.*171_*173del
NM_001289135.2:c.*171_*173del	NP_001276064.1:n.*171_*173del
NM_001289136.1:c.*171_*173del	NP_001276065.1:n.*171_*173del
NM_001289136.2:c.*171_*173del	NP_001276065.1:n.*171_*173del
NM_004787.2:c.*171_*173del	NP_004778.1:n.*171_*173del
NM_004787.3:c.*171_*173del	NP_004778.1:n.*171_*173del
XM_005248211.2:c.*171_*173del	XP_005248268.1:n.*171_*173del
XM_006713986.2:c.*171_*173del	XP_006714049.1:n.*171_*173del
XM_011513909.1:c.*171_*173del	XP_011512211.1:n.*171_*173del
XM_011513910.1:c.*171_*173del	XP_011512212.1:n.*171_*173del
XM_005248211.3:c.*171_*173del	XP_005248268.1:n.*171_*173del
XM_006713986.3:c.*171_*173del	XP_006714049.1:n.*171_*173del
XM_011513909.2:c.*171_*173del	XP_011512211.1:n.*171_*173del
XM_011513910.2:c.*171_*173del	XP_011512212.2:n.*171_*173del
XM_017008845.1:c.*171_*173del	XP_016864334.1:n.*171_*173del
NM_004787.4:c.*171_*173del MANE Select	NP_004778.1:n.*171_*173del
NM_001289135.3:c.*171_*173del	NP_001276064.1:n.*171_*173del
NM_001289136.3:c.*171_*173del	NP_001276065.1:n.*171_*173del