Canonical Allele Identifier: CA93471008

Gene: SLIT2

Linked Data

• dbSNP Id: rs970951148
• gnomAD v4: 4-20619331-G-A
• MyVariant Identifiers: chr4:g.20620954G>A (hg19) ; chr4:g.20619331G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.20619331G>A , CM000666.2:g.20619331G>A	GRCh38
NC_000004.11:g.20620954G>A , CM000666.1:g.20620954G>A	GRCh37
NC_000004.10:g.20230052G>A	NCBI36
NG_047105.1:g.372407G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504154.6:c.*322G>A MANE Select	ENSP00000422591.1:n.*322G>A
ENST00000504154.5:c.*322G>A	ENSP00000422591.1:n.*322G>A
ENST00000512993.1:c.237-1073G>A
ENST00000622093.4:c.*322G>A	ENSP00000482129.1:n.*322G>A
NM_001289135.1:c.*322G>A	NP_001276064.1:n.*322G>A
NM_001289135.2:c.*322G>A	NP_001276064.1:n.*322G>A
NM_001289136.1:c.*322G>A	NP_001276065.1:n.*322G>A
NM_001289136.2:c.*322G>A	NP_001276065.1:n.*322G>A
NM_004787.2:c.*322G>A	NP_004778.1:n.*322G>A
NM_004787.3:c.*322G>A	NP_004778.1:n.*322G>A
XM_005248211.2:c.*322G>A	XP_005248268.1:n.*322G>A
XM_006713986.2:c.*322G>A	XP_006714049.1:n.*322G>A
XM_011513909.1:c.*322G>A	XP_011512211.1:n.*322G>A
XM_011513910.1:c.*322G>A	XP_011512212.1:n.*322G>A
XM_005248211.3:c.*322G>A	XP_005248268.1:n.*322G>A
XM_006713986.3:c.*322G>A	XP_006714049.1:n.*322G>A
XM_011513909.2:c.*322G>A	XP_011512211.1:n.*322G>A
XM_011513910.2:c.*322G>A	XP_011512212.2:n.*322G>A
XM_017008845.1:c.*322G>A	XP_016864334.1:n.*322G>A
NM_004787.4:c.*322G>A MANE Select	NP_004778.1:n.*322G>A
NM_001289135.3:c.*322G>A	NP_001276064.1:n.*322G>A
NM_001289136.3:c.*322G>A	NP_001276065.1:n.*322G>A