Canonical Allele Identifier: CA792873016

Gene: SLIT2

Linked Data

• dbSNP Id: rs1236544848
• MyVariant Identifiers: chr4:g.20620971T>G (hg19) ; chr4:g.20619348T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.20619348T>G , CM000666.2:g.20619348T>G	GRCh38
NC_000004.11:g.20620971T>G , CM000666.1:g.20620971T>G	GRCh37
NC_000004.10:g.20230069T>G	NCBI36
NG_047105.1:g.372424T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504154.6:c.*339T>G MANE Select	ENSP00000422591.1:n.*339T>G
ENST00000504154.5:c.*339T>G	ENSP00000422591.1:n.*339T>G
ENST00000512993.1:c.237-1056T>G
ENST00000622093.4:c.*339T>G	ENSP00000482129.1:n.*339T>G
NM_001289135.1:c.*339T>G	NP_001276064.1:n.*339T>G
NM_001289135.2:c.*339T>G	NP_001276064.1:n.*339T>G
NM_001289136.1:c.*339T>G	NP_001276065.1:n.*339T>G
NM_001289136.2:c.*339T>G	NP_001276065.1:n.*339T>G
NM_004787.2:c.*339T>G	NP_004778.1:n.*339T>G
NM_004787.3:c.*339T>G	NP_004778.1:n.*339T>G
XM_005248211.2:c.*339T>G	XP_005248268.1:n.*339T>G
XM_006713986.2:c.*339T>G	XP_006714049.1:n.*339T>G
XM_011513909.1:c.*339T>G	XP_011512211.1:n.*339T>G
XM_011513910.1:c.*339T>G	XP_011512212.1:n.*339T>G
XM_005248211.3:c.*339T>G	XP_005248268.1:n.*339T>G
XM_006713986.3:c.*339T>G	XP_006714049.1:n.*339T>G
XM_011513909.2:c.*339T>G	XP_011512211.1:n.*339T>G
XM_011513910.2:c.*339T>G	XP_011512212.2:n.*339T>G
XM_017008845.1:c.*339T>G	XP_016864334.1:n.*339T>G
NM_004787.4:c.*339T>G MANE Select	NP_004778.1:n.*339T>G
NM_001289135.3:c.*339T>G	NP_001276064.1:n.*339T>G
NM_001289136.3:c.*339T>G	NP_001276065.1:n.*339T>G