Canonical Allele Identifier: CA2007101196
Gene: KIRREL3 HGNC NCBI
ST3GAL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126424726C= , CM000673.2:g.126424726C= GRCh38
NC_000011.9:g.126294621C= , CM000673.1:g.126294621C= GRCh37
NC_000011.8:g.125799831C= NCBI36
NG_012971.1:g.581146G=
NG_053025.1:g.74082C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525144.7:c.2191G= (KIRREL3) MANE Select ENSP00000435466.2:p.Val731=
ENST00000416561.6:c.2068G= (KIRREL3) ENSP00000408692.3:p.Val690=
ENST00000524834.5:n.629+15315C= (ST3GAL4)
ENST00000525144.6:c.2191G= (KIRREL3) ENSP00000435466.2:p.Val731=
ENST00000529097.6:c.2155G= (KIRREL3) ENSP00000434081.2:p.Val719=
NM_001301097.1:c.2155G= (KIRREL3) NP_001288026.1:p.Val719=
NM_032531.3:c.2191G= (KIRREL3) NP_115920.1:p.Val731=
XM_011542959.1:c.771+15315C= (ST3GAL4) XP_011541261.1:n.771+15315C=
XM_011542960.1:c.771+15315C= (ST3GAL4) XP_011541262.1:n.771+15315C=
XM_011542961.1:c.771+15315C= (ST3GAL4) XP_011541263.1:n.771+15315C=
XM_011542962.1:c.771+15315C= (ST3GAL4) XP_011541264.1:n.771+15315C=
XM_011543026.1:c.2284G= (KIRREL3) XP_011541328.1:p.Val762=
XM_011543027.1:c.2266G= (KIRREL3) XP_011541329.1:p.Val756=
XM_011543028.1:c.2266G= (KIRREL3) XP_011541330.1:p.Val756=
XM_011543029.1:c.2266G= (KIRREL3) XP_011541331.1:p.Val756=
XM_011543030.1:c.2209G= (KIRREL3) XP_011541332.1:p.Val737=
XM_011543031.1:c.2191G= (KIRREL3) XP_011541333.1:p.Val731=
XM_011543032.1:c.2173G= (KIRREL3) XP_011541334.1:p.Val725=
XM_011543033.1:c.2155G= (KIRREL3) XP_011541335.1:p.Val719=
XM_011543034.1:c.1624G= (KIRREL3) XP_011541336.1:p.Val542=
XM_011543026.2:c.2284G= (KIRREL3) XP_011541328.1:p.Val762=
XM_011543027.2:c.2266G= (KIRREL3) XP_011541329.1:p.Val756=
XM_011543028.2:c.2266G= (KIRREL3) XP_011541330.1:p.Val756=
XM_011543030.3:c.2209G= (KIRREL3) XP_011541332.1:p.Val737=
XM_011543031.2:c.2191G= (KIRREL3) XP_011541333.1:p.Val731=
XM_011543032.3:c.2173G= (KIRREL3) XP_011541334.1:p.Val725=
XM_017018419.1:c.2230G= (KIRREL3) XP_016873908.1:p.Val744=
XM_017018420.1:c.2191G= (KIRREL3) XP_016873909.1:p.Val731=
NM_032531.4:c.2191G= (KIRREL3) MANE Select NP_115920.1:p.Val731=