Canonical Allele Identifier: CA2616741723
Gene: KIRREL3 HGNC NCBI
ST3GAL4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126446917A>G , CM000673.2:g.126446917A>G GRCh38
NC_000011.9:g.126316812A>G , CM000673.1:g.126316812A>G GRCh37
NC_000011.8:g.125822022A>G NCBI36
NG_012971.1:g.558955T>C
NG_053025.1:g.96273A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000525144.7:c.998-31T>C (KIRREL3) MANE Select ENSP00000435466.2:n.998-31T>C
ENST00000416561.6:c.875-31T>C (KIRREL3) ENSP00000408692.3:n.875-31T>C
ENST00000525144.6:c.998-31T>C (KIRREL3) ENSP00000435466.2:n.998-31T>C
ENST00000525704.2:c.998-31T>C (KIRREL3) ENSP00000435094.2:n.998-31T>C
ENST00000529097.6:c.998-31T>C (KIRREL3) ENSP00000434081.2:n.998-31T>C
NM_001161707.1:c.998-31T>C (KIRREL3) NP_001155179.1:n.998-31T>C
NM_001301097.1:c.998-31T>C (KIRREL3) NP_001288026.1:n.998-31T>C
NM_032531.3:c.998-31T>C (KIRREL3) NP_115920.1:n.998-31T>C
XM_011542959.1:c.905+6598A>G (ST3GAL4) XP_011541261.1:n.905+6598A>G
XM_011542960.1:c.905+6598A>G (ST3GAL4) XP_011541262.1:n.905+6598A>G
XM_011542961.1:c.970-5684A>G (ST3GAL4) XP_011541263.1:n.970-5684A>G
XM_011542962.1:c.969+6534A>G (ST3GAL4) XP_011541264.1:n.969+6534A>G
XM_011543026.1:c.1016-31T>C (KIRREL3) XP_011541328.1:n.1016-31T>C
XM_011543027.1:c.998-31T>C (KIRREL3) XP_011541329.1:n.998-31T>C
XM_011543028.1:c.998-31T>C (KIRREL3) XP_011541330.1:n.998-31T>C
XM_011543029.1:c.998-31T>C (KIRREL3) XP_011541331.1:n.998-31T>C
XM_011543030.1:c.1016-31T>C (KIRREL3) XP_011541332.1:n.1016-31T>C
XM_011543031.1:c.998-31T>C (KIRREL3) XP_011541333.1:n.998-31T>C
XM_011543032.1:c.1016-31T>C (KIRREL3) XP_011541334.1:n.1016-31T>C
XM_011543033.1:c.998-31T>C (KIRREL3) XP_011541335.1:n.998-31T>C
XM_011543034.1:c.431-31T>C (KIRREL3) XP_011541336.1:n.431-31T>C
XM_011543026.2:c.1016-31T>C (KIRREL3) XP_011541328.1:n.1016-31T>C
XM_011543027.2:c.998-31T>C (KIRREL3) XP_011541329.1:n.998-31T>C
XM_011543028.2:c.998-31T>C (KIRREL3) XP_011541330.1:n.998-31T>C
XM_011543030.3:c.1016-31T>C (KIRREL3) XP_011541332.1:n.1016-31T>C
XM_011543031.2:c.998-31T>C (KIRREL3) XP_011541333.1:n.998-31T>C
XM_011543032.3:c.1016-31T>C (KIRREL3) XP_011541334.1:n.1016-31T>C
XM_017018419.1:c.998-31T>C (KIRREL3) XP_016873908.1:n.998-31T>C
XM_017018420.1:c.998-31T>C (KIRREL3) XP_016873909.1:n.998-31T>C
NM_032531.4:c.998-31T>C (KIRREL3) MANE Select NP_115920.1:n.998-31T>C