Canonical Allele Identifier: CA792872934

Gene: SLIT2

Linked Data

• dbSNP Id: rs1183287571
• MyVariant Identifiers: chr4:g.20620800_20620801insG (hg19) ; chr4:g.20619177_20619178insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.20619177_20619178insG , CM000666.2:g.20619177_20619178insG	GRCh38
NC_000004.11:g.20620800_20620801insG , CM000666.1:g.20620800_20620801insG	GRCh37
NC_000004.10:g.20229898_20229899insG	NCBI36
NG_047105.1:g.372253_372254insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504154.6:c.*168_*169insG MANE Select	ENSP00000422591.1:n.*168_*169insG
ENST00000273739.9:c.*168_*169insG	ENSP00000273739.5:n.*168_*169insG
ENST00000503837.5:c.4746_4747insG	ENSP00000422261.1:n.4746_4747insG
ENST00000504154.5:c.*168_*169insG	ENSP00000422591.1:n.*168_*169insG
ENST00000512993.1:c.237-1227_237-1226insG
ENST00000622093.4:c.*168_*169insG	ENSP00000482129.1:n.*168_*169insG
NM_001289135.1:c.*168_*169insG	NP_001276064.1:n.*168_*169insG
NM_001289135.2:c.*168_*169insG	NP_001276064.1:n.*168_*169insG
NM_001289136.1:c.*168_*169insG	NP_001276065.1:n.*168_*169insG
NM_001289136.2:c.*168_*169insG	NP_001276065.1:n.*168_*169insG
NM_004787.2:c.*168_*169insG	NP_004778.1:n.*168_*169insG
NM_004787.3:c.*168_*169insG	NP_004778.1:n.*168_*169insG
XM_005248211.2:c.*168_*169insG	XP_005248268.1:n.*168_*169insG
XM_006713986.2:c.*168_*169insG	XP_006714049.1:n.*168_*169insG
XM_011513909.1:c.*168_*169insG	XP_011512211.1:n.*168_*169insG
XM_011513910.1:c.*168_*169insG	XP_011512212.1:n.*168_*169insG
XM_005248211.3:c.*168_*169insG	XP_005248268.1:n.*168_*169insG
XM_006713986.3:c.*168_*169insG	XP_006714049.1:n.*168_*169insG
XM_011513909.2:c.*168_*169insG	XP_011512211.1:n.*168_*169insG
XM_011513910.2:c.*168_*169insG	XP_011512212.2:n.*168_*169insG
XM_017008845.1:c.*168_*169insG	XP_016864334.1:n.*168_*169insG
NM_004787.4:c.*168_*169insG MANE Select	NP_004778.1:n.*168_*169insG
NM_001289135.3:c.*168_*169insG	NP_001276064.1:n.*168_*169insG
NM_001289136.3:c.*168_*169insG	NP_001276065.1:n.*168_*169insG