Canonical Allele Identifier: CA383289462
Gene: KIRREL3 HGNC NCBI
ST3GAL4 HGNC NCBI
KIRREL3-AS1 HGNC NCBI

Linked Data

COSMIC: COSM364318

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126562846C>A , CM000673.2:g.126562846C>A GRCh38
NC_000011.9:g.126432741C>A , CM000673.1:g.126432741C>A GRCh37
NC_000011.8:g.125937951C>A NCBI36
NG_012971.1:g.443026G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000525144.7:c.122G>T (KIRREL3) MANE Select ENSP00000435466.2:p.Arg41Ile
ENST00000416561.6:c.-2G>T (KIRREL3) ENSP00000408692.3:n.-2G>T
ENST00000525144.6:c.122G>T (KIRREL3) ENSP00000435466.2:p.Arg41Ile
ENST00000525704.2:c.122G>T (KIRREL3) ENSP00000435094.2:p.Arg41Ile
ENST00000529097.6:c.122G>T (KIRREL3) ENSP00000434081.2:p.Arg41Ile
ENST00000533026.6:n.688G>T (KIRREL3)
ENST00000547738.5:n.778G>T (KIRREL3)
ENST00000549874.1:n.383G>T (KIRREL3)
NM_001161707.1:c.122G>T (KIRREL3) NP_001155179.1:p.Arg41Ile
NM_001301097.1:c.122G>T (KIRREL3) NP_001288026.1:p.Arg41Ile
NM_032531.3:c.122G>T (KIRREL3) NP_115920.1:p.Arg41Ile
XM_011542962.1:c.970-89935C>A (ST3GAL4) XP_011541264.1:n.970-89935C>A
XM_011543026.1:c.140G>T (KIRREL3) XP_011541328.1:p.Arg47Ile
XM_011543027.1:c.122G>T (KIRREL3) XP_011541329.1:p.Arg41Ile
XM_011543028.1:c.122G>T (KIRREL3) XP_011541330.1:p.Arg41Ile
XM_011543029.1:c.122G>T (KIRREL3) XP_011541331.1:p.Arg41Ile
XM_011543030.1:c.140G>T (KIRREL3) XP_011541332.1:p.Arg47Ile
XM_011543031.1:c.122G>T (KIRREL3) XP_011541333.1:p.Arg41Ile
XM_011543032.1:c.140G>T (KIRREL3) XP_011541334.1:p.Arg47Ile
XM_011543033.1:c.122G>T (KIRREL3) XP_011541335.1:p.Arg41Ile
XM_011543026.2:c.140G>T (KIRREL3) XP_011541328.1:p.Arg47Ile
XM_011543027.2:c.122G>T (KIRREL3) XP_011541329.1:p.Arg41Ile
XM_011543028.2:c.122G>T (KIRREL3) XP_011541330.1:p.Arg41Ile
XM_011543030.3:c.140G>T (KIRREL3) XP_011541332.1:p.Arg47Ile
XM_011543031.2:c.122G>T (KIRREL3) XP_011541333.1:p.Arg41Ile
XM_011543032.3:c.140G>T (KIRREL3) XP_011541334.1:p.Arg47Ile
XM_017018419.1:c.122G>T (KIRREL3) XP_016873908.1:p.Arg41Ile
XM_017018420.1:c.122G>T (KIRREL3) XP_016873909.1:p.Arg41Ile
NM_032531.4:c.122G>T (KIRREL3) MANE Select NP_115920.1:p.Arg41Ile
NR_174952.1:n.418+18602C>A (KIRREL3-AS1)