Canonical Allele Identifier: CA2259266539

Gene: IKZF3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39816455G>C , CM000679.2:g.39816455G>C	GRCh38
NC_000017.10:g.37972708G>C , CM000679.1:g.37972708G>C	GRCh37
NC_000017.9:g.35226234G>C	NCBI36
NG_029104.2:g.52734C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346872.8:c.163+12932C>G MANE Select	ENSP00000344544.3:n.163+12932C>G
ENST00000293068.9:c.163+12932C>G	ENSP00000462791.1:n.163+12932C>G
ENST00000346243.7:c.163+12932C>G	ENSP00000341977.3:n.163+12932C>G
ENST00000346872.7:c.163+12932C>G	ENSP00000344544.3:n.163+12932C>G
ENST00000348427.7:c.163+12932C>G	ENSP00000463505.1:n.163+12932C>G
ENST00000350532.7:c.163+12932C>G	ENSP00000344471.3:n.163+12932C>G
ENST00000351680.7:c.163+12932C>G	ENSP00000345622.3:n.163+12932C>G
ENST00000377944.7:c.163+12932C>G	ENSP00000367179.3:n.163+12932C>G
ENST00000377945.7:c.163+12932C>G	ENSP00000367180.3:n.163+12932C>G
ENST00000377952.6:c.163+12932C>G	ENSP00000367188.2:n.163+12932C>G
ENST00000377958.6:c.163+12932C>G	ENSP00000367194.2:n.163+12932C>G
ENST00000394189.6:c.163+12932C>G	ENSP00000377741.2:n.163+12932C>G
ENST00000439016.2:c.163+12932C>G	ENSP00000403027.2:n.163+12932C>G
ENST00000439167.6:c.61+15643C>G	ENSP00000403776.2:n.61+15643C>G
ENST00000467757.5:c.163+12932C>G	ENSP00000420463.1:n.163+12932C>G
ENST00000535189.5:c.61+15643C>G	ENSP00000438972.1:n.61+15643C>G
ENST00000623724.3:c.-705+12932C>G	ENSP00000485515.1:n.-705+12932C>G
NM_001257408.1:c.61+15643C>G	NP_001244337.1:n.61+15643C>G
NM_001257409.1:c.61+15643C>G	NP_001244338.1:n.61+15643C>G
NM_001257410.1:c.163+12932C>G	NP_001244339.1:n.163+12932C>G
NM_001257411.1:c.163+12932C>G	NP_001244340.1:n.163+12932C>G
NM_001257412.1:c.163+12932C>G	NP_001244341.1:n.163+12932C>G
NM_001257413.1:c.163+12932C>G	NP_001244342.1:n.163+12932C>G
NM_001257414.1:c.163+12932C>G	NP_001244343.1:n.163+12932C>G
NM_001284514.1:c.-705+12932C>G	NP_001271443.1:n.-705+12932C>G
NM_001284515.1:c.-537+12932C>G	NP_001271444.1:n.-537+12932C>G
NM_012481.4:c.163+12932C>G	NP_036613.2:n.163+12932C>G
NM_183228.2:c.163+12932C>G	NP_899051.1:n.163+12932C>G
NM_183229.2:c.163+12932C>G	NP_899052.1:n.163+12932C>G
NM_183230.2:c.163+12932C>G	NP_899053.1:n.163+12932C>G
NM_183231.2:c.163+12932C>G	NP_899054.1:n.163+12932C>G
NM_183232.2:c.163+12932C>G	NP_899055.1:n.163+12932C>G
NM_012481.5:c.163+12932C>G MANE Select	NP_036613.2:n.163+12932C>G
NM_001257408.2:c.61+15643C>G	NP_001244337.1:n.61+15643C>G
NM_001257409.2:c.61+15643C>G	NP_001244338.1:n.61+15643C>G
NM_001257410.2:c.163+12932C>G	NP_001244339.1:n.163+12932C>G
NM_001257411.2:c.163+12932C>G	NP_001244340.1:n.163+12932C>G
NM_001257412.2:c.163+12932C>G	NP_001244341.1:n.163+12932C>G
NM_001257413.2:c.163+12932C>G	NP_001244342.1:n.163+12932C>G
NM_001257414.2:c.163+12932C>G	NP_001244343.1:n.163+12932C>G
NM_001284515.2:c.-537+12932C>G	NP_001271444.1:n.-537+12932C>G
NM_183228.3:c.163+12932C>G	NP_899051.1:n.163+12932C>G
NM_183229.3:c.163+12932C>G	NP_899052.1:n.163+12932C>G
NM_183230.3:c.163+12932C>G	NP_899053.1:n.163+12932C>G
NM_183231.3:c.163+12932C>G	NP_899054.1:n.163+12932C>G
NM_183232.3:c.163+12932C>G	NP_899055.1:n.163+12932C>G
NM_001284514.2:c.-705+12932C>G	NP_001271443.1:n.-705+12932C>G