Canonical Allele Identifier: CA477524889

Gene: KIRREL3 ST3GAL4

Linked Data

• MyVariant Identifiers: chr11:g.126316780A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126446885A>G , CM000673.2:g.126446885A>G	GRCh38
NC_000011.9:g.126316780A>G , CM000673.1:g.126316780A>G	GRCh37
NC_000011.8:g.125821990A>G	NCBI36
NG_012971.1:g.558987T>C
NG_053025.1:g.96241A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525144.7:c.999T>C (KIRREL3) MANE Select	ENSP00000435466.2:p.Phe333=
ENST00000416561.6:c.876T>C (KIRREL3)	ENSP00000408692.3:p.Phe292=
ENST00000525144.6:c.999T>C (KIRREL3)	ENSP00000435466.2:p.Phe333=
ENST00000525704.2:c.999T>C (KIRREL3)	ENSP00000435094.2:p.Phe333=
ENST00000529097.6:c.999T>C (KIRREL3)	ENSP00000434081.2:p.Phe333=
NM_001161707.1:c.999T>C (KIRREL3)	NP_001155179.1:p.Phe333=
NM_001301097.1:c.999T>C (KIRREL3)	NP_001288026.1:p.Phe333=
NM_032531.3:c.999T>C (KIRREL3)	NP_115920.1:p.Phe333=
XM_011542959.1:c.905+6566A>G (ST3GAL4)	XP_011541261.1:n.905+6566A>G
XM_011542960.1:c.905+6566A>G (ST3GAL4)	XP_011541262.1:n.905+6566A>G
XM_011542961.1:c.970-5716A>G (ST3GAL4)	XP_011541263.1:n.970-5716A>G
XM_011542962.1:c.969+6502A>G (ST3GAL4)	XP_011541264.1:n.969+6502A>G
XM_011543026.1:c.1017T>C (KIRREL3)	XP_011541328.1:p.Phe339=
XM_011543027.1:c.999T>C (KIRREL3)	XP_011541329.1:p.Phe333=
XM_011543028.1:c.999T>C (KIRREL3)	XP_011541330.1:p.Phe333=
XM_011543029.1:c.999T>C (KIRREL3)	XP_011541331.1:p.Phe333=
XM_011543030.1:c.1017T>C (KIRREL3)	XP_011541332.1:p.Phe339=
XM_011543031.1:c.999T>C (KIRREL3)	XP_011541333.1:p.Phe333=
XM_011543032.1:c.1017T>C (KIRREL3)	XP_011541334.1:p.Phe339=
XM_011543033.1:c.999T>C (KIRREL3)	XP_011541335.1:p.Phe333=
XM_011543034.1:c.432T>C (KIRREL3)	XP_011541336.1:p.Phe144=
XM_011543026.2:c.1017T>C (KIRREL3)	XP_011541328.1:p.Phe339=
XM_011543027.2:c.999T>C (KIRREL3)	XP_011541329.1:p.Phe333=
XM_011543028.2:c.999T>C (KIRREL3)	XP_011541330.1:p.Phe333=
XM_011543030.3:c.1017T>C (KIRREL3)	XP_011541332.1:p.Phe339=
XM_011543031.2:c.999T>C (KIRREL3)	XP_011541333.1:p.Phe333=
XM_011543032.3:c.1017T>C (KIRREL3)	XP_011541334.1:p.Phe339=
XM_017018419.1:c.999T>C (KIRREL3)	XP_016873908.1:p.Phe333=
XM_017018420.1:c.999T>C (KIRREL3)	XP_016873909.1:p.Phe333=
NM_032531.4:c.999T>C (KIRREL3) MANE Select	NP_115920.1:p.Phe333=