Canonical Allele Identifier: CA792873026

Gene: SLIT2

Linked Data

• dbSNP Id: rs1316184896
• gnomAD v3: 4-20619351-GA-G
• gnomAD v4: 4-20619351-GA-G
• MyVariant Identifiers: chr4:g.20620975del (hg19) ; chr4:g.20619352del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.20619354del , CM000666.2:g.20619354del	GRCh38
NC_000004.11:g.20620977del , CM000666.1:g.20620977del	GRCh37
NC_000004.10:g.20230075del	NCBI36
NG_047105.1:g.372430del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504154.6:c.*345del MANE Select	ENSP00000422591.1:n.*345del
ENST00000504154.5:c.*345del	ENSP00000422591.1:n.*345del
ENST00000512993.1:c.237-1050del
ENST00000622093.4:c.*345del	ENSP00000482129.1:n.*345del
NM_001289135.1:c.*345del	NP_001276064.1:n.*345del
NM_001289135.2:c.*345del	NP_001276064.1:n.*345del
NM_001289136.1:c.*345del	NP_001276065.1:n.*345del
NM_001289136.2:c.*345del	NP_001276065.1:n.*345del
NM_004787.2:c.*345del	NP_004778.1:n.*345del
NM_004787.3:c.*345del	NP_004778.1:n.*345del
XM_005248211.2:c.*345del	XP_005248268.1:n.*345del
XM_006713986.2:c.*345del	XP_006714049.1:n.*345del
XM_011513909.1:c.*345del	XP_011512211.1:n.*345del
XM_011513910.1:c.*345del	XP_011512212.1:n.*345del
XM_005248211.3:c.*345del	XP_005248268.1:n.*345del
XM_006713986.3:c.*345del	XP_006714049.1:n.*345del
XM_011513909.2:c.*345del	XP_011512211.1:n.*345del
XM_011513910.2:c.*345del	XP_011512212.2:n.*345del
XM_017008845.1:c.*345del	XP_016864334.1:n.*345del
NM_004787.4:c.*345del MANE Select	NP_004778.1:n.*345del
NM_001289135.3:c.*345del	NP_001276064.1:n.*345del
NM_001289136.3:c.*345del	NP_001276065.1:n.*345del