Canonical Allele Identifier: CA1443092312
Gene: SLIT2 HGNC NCBI

Linked Data

dbSNP Id: rs1729920844

Genomic Alleles

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

Transcript Alleles

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