Canonical Allele Identifier: CA549920017
Gene: SLIT2 HGNC NCBI

Linked Data

dbSNP Id: rs1436504578

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.20619080_20619081del , CM000666.2:g.20619080_20619081del GRCh38
NC_000004.11:g.20620703_20620704del , CM000666.1:g.20620703_20620704del GRCh37
NC_000004.10:g.20229801_20229802del NCBI36
NG_047105.1:g.372156_372157del

Transcript Alleles

HGVS Amino-acid Change
ENST00000504154.6:c.*71_*72del MANE Select ENSP00000422591.1:n.*71_*72del
ENST00000273739.9:c.*71_*72del ENSP00000273739.5:n.*71_*72del
ENST00000503823.5:c.*71_*72del ENSP00000427548.1:n.*71_*72del
ENST00000503837.5:c.4649_4650del ENSP00000422261.1:n.4649_4650del
ENST00000504154.5:c.*71_*72del ENSP00000422591.1:n.*71_*72del
ENST00000508541.1:n.2861_2862del
ENST00000512993.1:c.237-1324_237-1323del
ENST00000622093.4:c.*71_*72del ENSP00000482129.1:n.*71_*72del
NM_001289135.1:c.*71_*72del NP_001276064.1:n.*71_*72del
NM_001289135.2:c.*71_*72del NP_001276064.1:n.*71_*72del
NM_001289136.1:c.*71_*72del NP_001276065.1:n.*71_*72del
NM_001289136.2:c.*71_*72del NP_001276065.1:n.*71_*72del
NM_004787.2:c.*71_*72del NP_004778.1:n.*71_*72del
NM_004787.3:c.*71_*72del NP_004778.1:n.*71_*72del
XM_005248211.2:c.*71_*72del XP_005248268.1:n.*71_*72del
XM_006713986.2:c.*71_*72del XP_006714049.1:n.*71_*72del
XM_011513909.1:c.*71_*72del XP_011512211.1:n.*71_*72del
XM_011513910.1:c.*71_*72del XP_011512212.1:n.*71_*72del
XM_005248211.3:c.*71_*72del XP_005248268.1:n.*71_*72del
XM_006713986.3:c.*71_*72del XP_006714049.1:n.*71_*72del
XM_011513909.2:c.*71_*72del XP_011512211.1:n.*71_*72del
XM_011513910.2:c.*71_*72del XP_011512212.2:n.*71_*72del
XM_017008845.1:c.*71_*72del XP_016864334.1:n.*71_*72del
NM_004787.4:c.*71_*72del MANE Select NP_004778.1:n.*71_*72del
NM_001289135.3:c.*71_*72del NP_001276064.1:n.*71_*72del
NM_001289136.3:c.*71_*72del NP_001276065.1:n.*71_*72del