Canonical Allele Identifier: CA1443092303
Gene: SLIT2 HGNC NCBI

Linked Data

dbSNP Id: rs1729919641
gnomAD v4: 4-20619314-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.20619314A>G , CM000666.2:g.20619314A>G GRCh38
NC_000004.11:g.20620937A>G , CM000666.1:g.20620937A>G GRCh37
NC_000004.10:g.20230035A>G NCBI36
NG_047105.1:g.372390A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000504154.6:c.*305A>G MANE Select ENSP00000422591.1:n.*305A>G
ENST00000504154.5:c.*305A>G ENSP00000422591.1:n.*305A>G
ENST00000512993.1:c.237-1090A>G
ENST00000622093.4:c.*305A>G ENSP00000482129.1:n.*305A>G
NM_001289135.1:c.*305A>G NP_001276064.1:n.*305A>G
NM_001289135.2:c.*305A>G NP_001276064.1:n.*305A>G
NM_001289136.1:c.*305A>G NP_001276065.1:n.*305A>G
NM_001289136.2:c.*305A>G NP_001276065.1:n.*305A>G
NM_004787.2:c.*305A>G NP_004778.1:n.*305A>G
NM_004787.3:c.*305A>G NP_004778.1:n.*305A>G
XM_005248211.2:c.*305A>G XP_005248268.1:n.*305A>G
XM_006713986.2:c.*305A>G XP_006714049.1:n.*305A>G
XM_011513909.1:c.*305A>G XP_011512211.1:n.*305A>G
XM_011513910.1:c.*305A>G XP_011512212.1:n.*305A>G
XM_005248211.3:c.*305A>G XP_005248268.1:n.*305A>G
XM_006713986.3:c.*305A>G XP_006714049.1:n.*305A>G
XM_011513909.2:c.*305A>G XP_011512211.1:n.*305A>G
XM_011513910.2:c.*305A>G XP_011512212.2:n.*305A>G
XM_017008845.1:c.*305A>G XP_016864334.1:n.*305A>G
NM_004787.4:c.*305A>G MANE Select NP_004778.1:n.*305A>G
NM_001289135.3:c.*305A>G NP_001276064.1:n.*305A>G
NM_001289136.3:c.*305A>G NP_001276065.1:n.*305A>G