Canonical Allele Identifier: CA2670167103

Gene: SLIT2

Linked Data

• gnomAD v4: 4-20619078-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.20619078C>G , CM000666.2:g.20619078C>G	GRCh38
NC_000004.11:g.20620701C>G , CM000666.1:g.20620701C>G	GRCh37
NC_000004.10:g.20229799C>G	NCBI36
NG_047105.1:g.372154C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504154.6:c.*69C>G MANE Select	ENSP00000422591.1:n.*69C>G
ENST00000273739.9:c.*69C>G	ENSP00000273739.5:n.*69C>G
ENST00000503823.5:c.*69C>G	ENSP00000427548.1:n.*69C>G
ENST00000503837.5:c.4647C>G	ENSP00000422261.1:n.4647C>G
ENST00000504154.5:c.*69C>G	ENSP00000422591.1:n.*69C>G
ENST00000508541.1:n.2859C>G
ENST00000512993.1:c.237-1326C>G
ENST00000622093.4:c.*69C>G	ENSP00000482129.1:n.*69C>G
NM_001289135.1:c.*69C>G	NP_001276064.1:n.*69C>G
NM_001289135.2:c.*69C>G	NP_001276064.1:n.*69C>G
NM_001289136.1:c.*69C>G	NP_001276065.1:n.*69C>G
NM_001289136.2:c.*69C>G	NP_001276065.1:n.*69C>G
NM_004787.2:c.*69C>G	NP_004778.1:n.*69C>G
NM_004787.3:c.*69C>G	NP_004778.1:n.*69C>G
XM_005248211.2:c.*69C>G	XP_005248268.1:n.*69C>G
XM_006713986.2:c.*69C>G	XP_006714049.1:n.*69C>G
XM_011513909.1:c.*69C>G	XP_011512211.1:n.*69C>G
XM_011513910.1:c.*69C>G	XP_011512212.1:n.*69C>G
XM_005248211.3:c.*69C>G	XP_005248268.1:n.*69C>G
XM_006713986.3:c.*69C>G	XP_006714049.1:n.*69C>G
XM_011513909.2:c.*69C>G	XP_011512211.1:n.*69C>G
XM_011513910.2:c.*69C>G	XP_011512212.2:n.*69C>G
XM_017008845.1:c.*69C>G	XP_016864334.1:n.*69C>G
NM_004787.4:c.*69C>G MANE Select	NP_004778.1:n.*69C>G
NM_001289135.3:c.*69C>G	NP_001276064.1:n.*69C>G
NM_001289136.3:c.*69C>G	NP_001276065.1:n.*69C>G