Canonical Allele Identifier: CA2007112024

Gene: KIRREL3 ST3GAL4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126446930_126446931delinsGC , CM000673.2:g.126446930_126446931delinsGC	GRCh38
NC_000011.9:g.126316825_126316826delinsGC , CM000673.1:g.126316825_126316826delinsGC	GRCh37
NC_000011.8:g.125822035_125822036delinsGC	NCBI36
NG_012971.1:g.558941_558942delinsGC
NG_053025.1:g.96286_96287delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525144.7:c.998-45_998-44delinsGC (KIRREL3) MANE Select	ENSP00000435466.2:n.998-45_998-44delinsGC
ENST00000416561.6:c.875-45_875-44delinsGC (KIRREL3)	ENSP00000408692.3:n.875-45_875-44delinsGC
ENST00000525144.6:c.998-45_998-44delinsGC (KIRREL3)	ENSP00000435466.2:n.998-45_998-44delinsGC
ENST00000525704.2:c.998-45_998-44delinsGC (KIRREL3)	ENSP00000435094.2:n.998-45_998-44delinsGC
ENST00000529097.6:c.998-45_998-44delinsGC (KIRREL3)	ENSP00000434081.2:n.998-45_998-44delinsGC
NM_001161707.1:c.998-45_998-44delinsGC (KIRREL3)	NP_001155179.1:n.998-45_998-44delinsGC
NM_001301097.1:c.998-45_998-44delinsGC (KIRREL3)	NP_001288026.1:n.998-45_998-44delinsGC
NM_032531.3:c.998-45_998-44delinsGC (KIRREL3)	NP_115920.1:n.998-45_998-44delinsGC
XM_011542959.1:c.905+6611_905+6612delinsGC (ST3GAL4)	XP_011541261.1:n.905+6611_905+6612delinsGC
XM_011542960.1:c.905+6611_905+6612delinsGC (ST3GAL4)	XP_011541262.1:n.905+6611_905+6612delinsGC
XM_011542961.1:c.970-5671_970-5670delinsGC (ST3GAL4)	XP_011541263.1:n.970-5671_970-5670delinsGC
XM_011542962.1:c.969+6547_969+6548delinsGC (ST3GAL4)	XP_011541264.1:n.969+6547_969+6548delinsGC
XM_011543026.1:c.1016-45_1016-44delinsGC (KIRREL3)	XP_011541328.1:n.1016-45_1016-44delinsGC
XM_011543027.1:c.998-45_998-44delinsGC (KIRREL3)	XP_011541329.1:n.998-45_998-44delinsGC
XM_011543028.1:c.998-45_998-44delinsGC (KIRREL3)	XP_011541330.1:n.998-45_998-44delinsGC
XM_011543029.1:c.998-45_998-44delinsGC (KIRREL3)	XP_011541331.1:n.998-45_998-44delinsGC
XM_011543030.1:c.1016-45_1016-44delinsGC (KIRREL3)	XP_011541332.1:n.1016-45_1016-44delinsGC
XM_011543031.1:c.998-45_998-44delinsGC (KIRREL3)	XP_011541333.1:n.998-45_998-44delinsGC
XM_011543032.1:c.1016-45_1016-44delinsGC (KIRREL3)	XP_011541334.1:n.1016-45_1016-44delinsGC
XM_011543033.1:c.998-45_998-44delinsGC (KIRREL3)	XP_011541335.1:n.998-45_998-44delinsGC
XM_011543034.1:c.431-45_431-44delinsGC (KIRREL3)	XP_011541336.1:n.431-45_431-44delinsGC
XM_011543026.2:c.1016-45_1016-44delinsGC (KIRREL3)	XP_011541328.1:n.1016-45_1016-44delinsGC
XM_011543027.2:c.998-45_998-44delinsGC (KIRREL3)	XP_011541329.1:n.998-45_998-44delinsGC
XM_011543028.2:c.998-45_998-44delinsGC (KIRREL3)	XP_011541330.1:n.998-45_998-44delinsGC
XM_011543030.3:c.1016-45_1016-44delinsGC (KIRREL3)	XP_011541332.1:n.1016-45_1016-44delinsGC
XM_011543031.2:c.998-45_998-44delinsGC (KIRREL3)	XP_011541333.1:n.998-45_998-44delinsGC
XM_011543032.3:c.1016-45_1016-44delinsGC (KIRREL3)	XP_011541334.1:n.1016-45_1016-44delinsGC
XM_017018419.1:c.998-45_998-44delinsGC (KIRREL3)	XP_016873908.1:n.998-45_998-44delinsGC
XM_017018420.1:c.998-45_998-44delinsGC (KIRREL3)	XP_016873909.1:n.998-45_998-44delinsGC
NM_032531.4:c.998-45_998-44delinsGC (KIRREL3) MANE Select	NP_115920.1:n.998-45_998-44delinsGC