Canonical Allele Identifier: CA237609014

Gene: IKZF4

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56018703T>G , CM000674.2:g.56018703T>G	GRCh38
NC_000012.11:g.56412487T>G , CM000674.1:g.56412487T>G	GRCh37
NC_000012.10:g.54698754T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262032.9:c.-162+526T>G	ENSP00000262032.5:n.-162+526T>G
ENST00000548601.5:n.118+526T>G
ENST00000550860.5:n.414+526T>G
ENST00000552689.1:c.-159+526T>G	ENSP00000449168.1:n.-159+526T>G
XM_005269086.3:c.21+526T>G	XP_005269143.1:n.21+526T>G
XM_005269089.1:c.40+526T>G	XP_005269146.1:n.40+526T>G
XM_005269090.3:c.40+526T>G	XP_005269147.1:n.40+526T>G
XM_005269091.3:c.40+526T>G	XP_005269148.1:n.40+526T>G
XM_005269092.3:c.40+526T>G	XP_005269149.1:n.40+526T>G
XM_006719561.2:c.21+526T>G	XP_006719624.1:n.21+526T>G
XM_011538664.1:c.21+526T>G	XP_011536966.1:n.21+526T>G
XM_011538665.1:c.21+526T>G	XP_011536967.1:n.21+526T>G
XM_011538666.1:c.21+526T>G	XP_011536968.1:n.21+526T>G
XM_011538669.1:c.40+526T>G	XP_011536971.1:n.40+526T>G
NM_001351091.1:c.40+526T>G	NP_001338020.1:n.40+526T>G
NR_135023.1:n.63+6326A>C
XM_005269089.2:c.40+526T>G	XP_005269146.1:n.40+526T>G
XM_011538669.2:c.40+526T>G	XP_011536971.1:n.40+526T>G
XM_017019805.1:c.-162+526T>G	XP_016875294.1:n.-162+526T>G
XM_017019806.1:c.-162+526T>G	XP_016875295.1:n.-162+526T>G
XM_017019807.1:c.-159+526T>G	XP_016875296.1:n.-159+526T>G
XM_017019808.1:c.-162+526T>G	XP_016875297.1:n.-162+526T>G
XM_017019809.1:c.-159+526T>G	XP_016875298.1:n.-159+526T>G
XM_017019810.1:c.-162+526T>G	XP_016875299.1:n.-162+526T>G
XM_017019811.1:c.-159+526T>G	XP_016875300.1:n.-159+526T>G
XM_017019812.1:c.21+526T>G	XP_016875301.1:n.21+526T>G
XM_017019813.1:c.21+526T>G	XP_016875302.1:n.21+526T>G
XM_017019814.1:c.40+526T>G	XP_016875303.1:n.40+526T>G
XM_017019815.1:c.40+526T>G	XP_016875304.1:n.40+526T>G
XM_017019816.1:c.40+526T>G	XP_016875305.1:n.40+526T>G
XM_024449128.1:c.-171+526T>G	XP_024304896.1:n.-171+526T>G
XM_024449129.1:c.-224+526T>G	XP_024304897.1:n.-224+526T>G
NM_001351089.2:c.-162+526T>G	NP_001338018.1:n.-162+526T>G
NM_001351091.2:c.40+526T>G	NP_001338020.1:n.40+526T>G