Canonical Allele Identifier: CA13590095

Gene: IKZF4

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56023144A>C , CM000674.2:g.56023144A>C	GRCh38
NC_000012.11:g.56416928A>C , CM000674.1:g.56416928A>C	GRCh37
NC_000012.10:g.54703195A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547167.6:c.88-527A>C MANE Select	ENSP00000448419.1:n.88-527A>C
ENST00000262032.9:c.88-527A>C	ENSP00000262032.5:n.88-527A>C
ENST00000431367.6:c.88-527A>C	ENSP00000412101.3:n.88-527A>C
ENST00000547167.5:c.88-527A>C	ENSP00000448419.1:n.88-527A>C
ENST00000547668.5:n.236-527A>C
ENST00000547791.2:c.46+1694A>C	ENSP00000450020.1:n.46+1694A>C
ENST00000548601.5:n.119-1910A>C
ENST00000549519.5:n.97-1518A>C
ENST00000550860.5:n.415-1910A>C
ENST00000551103.5:c.87+1564A>C	ENSP00000449857.1:n.87+1564A>C
ENST00000551701.5:n.60-527A>C
NM_022465.3:c.88-527A>C	NP_071910.3:n.88-527A>C
XM_005269086.3:c.22-527A>C	XP_005269143.1:n.22-527A>C
XM_005269089.1:c.41-1910A>C	XP_005269146.1:n.41-1910A>C
XM_005269090.3:c.41-1910A>C	XP_005269147.1:n.41-1910A>C
XM_005269091.3:c.41-1910A>C	XP_005269148.1:n.41-1910A>C
XM_005269092.3:c.41-1910A>C	XP_005269149.1:n.41-1910A>C
XM_005269093.1:c.-126+1564A>C	XP_005269150.1:n.-126+1564A>C
XM_006719561.2:c.22-527A>C	XP_006719624.1:n.22-527A>C
XM_011538664.1:c.22-527A>C	XP_011536966.1:n.22-527A>C
XM_011538665.1:c.22-527A>C	XP_011536967.1:n.22-527A>C
XM_011538666.1:c.22-527A>C	XP_011536968.1:n.22-527A>C
XM_011538669.1:c.41-1910A>C	XP_011536971.1:n.41-1910A>C
XM_011538670.1:c.-122+1564A>C	XP_011536972.1:n.-122+1564A>C
XR_944989.1:n.555-2847T>G
XR_944990.1:n.436-2847T>G
NM_001351089.1:c.88-527A>C	NP_001338018.1:n.88-527A>C
NM_001351090.1:c.46+1694A>C	NP_001338019.1:n.46+1694A>C
NM_001351091.1:c.41-1910A>C	NP_001338020.1:n.41-1910A>C
NM_001351092.1:c.-126+1564A>C	NP_001338021.1:n.-126+1564A>C
NR_135023.1:n.63+1885T>G
XM_005269089.2:c.41-1910A>C	XP_005269146.1:n.41-1910A>C
XM_011538669.2:c.41-1910A>C	XP_011536971.1:n.41-1910A>C
XM_017019805.1:c.88-527A>C	XP_016875294.1:n.88-527A>C
XM_017019806.1:c.88-527A>C	XP_016875295.1:n.88-527A>C
XM_017019807.1:c.88-527A>C	XP_016875296.1:n.88-527A>C
XM_017019808.1:c.88-527A>C	XP_016875297.1:n.88-527A>C
XM_017019809.1:c.88-527A>C	XP_016875298.1:n.88-527A>C
XM_017019810.1:c.88-527A>C	XP_016875299.1:n.88-527A>C
XM_017019811.1:c.88-527A>C	XP_016875300.1:n.88-527A>C
XM_017019812.1:c.22-527A>C	XP_016875301.1:n.22-527A>C
XM_017019813.1:c.22-527A>C	XP_016875302.1:n.22-527A>C
XM_017019814.1:c.41-1910A>C	XP_016875303.1:n.41-1910A>C
XM_017019815.1:c.41-1910A>C	XP_016875304.1:n.41-1910A>C
XM_017019816.1:c.41-1910A>C	XP_016875305.1:n.41-1910A>C
XM_024449128.1:c.-72-527A>C	XP_024304896.1:n.-72-527A>C
XM_024449129.1:c.-125-1910A>C	XP_024304897.1:n.-125-1910A>C
XM_024449130.1:c.-1887A>C	XP_024304898.1:n.-1887A>C
XM_024449131.1:c.-914A>C	XP_024304899.1:n.-914A>C
XR_944989.3:n.846-2847T>G
XR_944990.3:n.727-2847T>G
NM_001351089.2:c.88-527A>C	NP_001338018.1:n.88-527A>C
NM_022465.4:c.88-527A>C MANE Select	NP_071910.3:n.88-527A>C
NM_001351091.2:c.41-1910A>C	NP_001338020.1:n.41-1910A>C
NM_001351092.2:c.-126+1564A>C	NP_001338021.1:n.-126+1564A>C