Canonical Allele Identifier: CA549920024

Gene: SLIT2

Linked Data

• dbSNP Id: rs1406630446
• gnomAD v2: 4-20620789-G-A
• gnomAD v3: 4-20619166-G-A
• gnomAD v4: 4-20619166-G-A
• MyVariant Identifiers: chr4:g.20620789G>A (hg19) ; chr4:g.20620789_20620791delinsAAA (hg19) ; chr4:g.20619166G>A (hg38) ; chr4:g.20619166_20619168delinsAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.20619166G>A , CM000666.2:g.20619166G>A	GRCh38
NC_000004.11:g.20620789G>A , CM000666.1:g.20620789G>A	GRCh37
NC_000004.10:g.20229887G>A	NCBI36
NG_047105.1:g.372242G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504154.6:c.*157G>A MANE Select	ENSP00000422591.1:n.*157G>A
ENST00000273739.9:c.*157G>A	ENSP00000273739.5:n.*157G>A
ENST00000503837.5:c.4735G>A	ENSP00000422261.1:n.4735G>A
ENST00000504154.5:c.*157G>A	ENSP00000422591.1:n.*157G>A
ENST00000508541.1:n.2947G>A
ENST00000512993.1:c.237-1238G>A
ENST00000622093.4:c.*157G>A	ENSP00000482129.1:n.*157G>A
NM_001289135.1:c.*157G>A	NP_001276064.1:n.*157G>A
NM_001289135.2:c.*157G>A	NP_001276064.1:n.*157G>A
NM_001289136.1:c.*157G>A	NP_001276065.1:n.*157G>A
NM_001289136.2:c.*157G>A	NP_001276065.1:n.*157G>A
NM_004787.2:c.*157G>A	NP_004778.1:n.*157G>A
NM_004787.3:c.*157G>A	NP_004778.1:n.*157G>A
XM_005248211.2:c.*157G>A	XP_005248268.1:n.*157G>A
XM_006713986.2:c.*157G>A	XP_006714049.1:n.*157G>A
XM_011513909.1:c.*157G>A	XP_011512211.1:n.*157G>A
XM_011513910.1:c.*157G>A	XP_011512212.1:n.*157G>A
XM_005248211.3:c.*157G>A	XP_005248268.1:n.*157G>A
XM_006713986.3:c.*157G>A	XP_006714049.1:n.*157G>A
XM_011513909.2:c.*157G>A	XP_011512211.1:n.*157G>A
XM_011513910.2:c.*157G>A	XP_011512212.2:n.*157G>A
XM_017008845.1:c.*157G>A	XP_016864334.1:n.*157G>A
NM_004787.4:c.*157G>A MANE Select	NP_004778.1:n.*157G>A
NM_001289135.3:c.*157G>A	NP_001276064.1:n.*157G>A
NM_001289136.3:c.*157G>A	NP_001276065.1:n.*157G>A