Canonical Allele Identifier: CA1443092210

Gene: SLIT2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.20619124_20619130delinsCTTATTT , CM000666.2:g.20619124_20619130delinsCTTATTT	GRCh38
NC_000004.11:g.20620747_20620753delinsCTTATTT , CM000666.1:g.20620747_20620753delinsCTTATTT	GRCh37
NC_000004.10:g.20229845_20229851delinsCTTATTT	NCBI36
NG_047105.1:g.372200_372206delinsCTTATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504154.6:c.*115_*121delinsCTTATTT MANE Select	ENSP00000422591.1:n.*115_*121delinsCTTATTT
ENST00000273739.9:c.*115_*121delinsCTTATTT	ENSP00000273739.5:n.*115_*121delinsCTTATTT
ENST00000503837.5:c.4693_4699delinsCTTATTT	ENSP00000422261.1:n.4693_4699delinsCTTATTT
ENST00000504154.5:c.*115_*121delinsCTTATTT	ENSP00000422591.1:n.*115_*121delinsCTTATTT
ENST00000508541.1:n.2905_2911delinsCTTATTT
ENST00000512993.1:c.237-1280_237-1274delinsCTTATTT
ENST00000622093.4:c.*115_*121delinsCTTATTT	ENSP00000482129.1:n.*115_*121delinsCTTATTT
NM_001289135.1:c.*115_*121delinsCTTATTT	NP_001276064.1:n.*115_*121delinsCTTATTT
NM_001289135.2:c.*115_*121delinsCTTATTT	NP_001276064.1:n.*115_*121delinsCTTATTT
NM_001289136.1:c.*115_*121delinsCTTATTT	NP_001276065.1:n.*115_*121delinsCTTATTT
NM_001289136.2:c.*115_*121delinsCTTATTT	NP_001276065.1:n.*115_*121delinsCTTATTT
NM_004787.2:c.*115_*121delinsCTTATTT	NP_004778.1:n.*115_*121delinsCTTATTT
NM_004787.3:c.*115_*121delinsCTTATTT	NP_004778.1:n.*115_*121delinsCTTATTT
XM_005248211.2:c.*115_*121delinsCTTATTT	XP_005248268.1:n.*115_*121delinsCTTATTT
XM_006713986.2:c.*115_*121delinsCTTATTT	XP_006714049.1:n.*115_*121delinsCTTATTT
XM_011513909.1:c.*115_*121delinsCTTATTT	XP_011512211.1:n.*115_*121delinsCTTATTT
XM_011513910.1:c.*115_*121delinsCTTATTT	XP_011512212.1:n.*115_*121delinsCTTATTT
XM_005248211.3:c.*115_*121delinsCTTATTT	XP_005248268.1:n.*115_*121delinsCTTATTT
XM_006713986.3:c.*115_*121delinsCTTATTT	XP_006714049.1:n.*115_*121delinsCTTATTT
XM_011513909.2:c.*115_*121delinsCTTATTT	XP_011512211.1:n.*115_*121delinsCTTATTT
XM_011513910.2:c.*115_*121delinsCTTATTT	XP_011512212.2:n.*115_*121delinsCTTATTT
XM_017008845.1:c.*115_*121delinsCTTATTT	XP_016864334.1:n.*115_*121delinsCTTATTT
NM_004787.4:c.*115_*121delinsCTTATTT MANE Select	NP_004778.1:n.*115_*121delinsCTTATTT
NM_001289135.3:c.*115_*121delinsCTTATTT	NP_001276064.1:n.*115_*121delinsCTTATTT
NM_001289136.3:c.*115_*121delinsCTTATTT	NP_001276065.1:n.*115_*121delinsCTTATTT