Canonical Allele Identifier: CA350787964

Gene: IKZF2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.213049830C>G , CM000664.2:g.213049830C>G	GRCh38
NC_000002.11:g.213914554C>G , CM000664.1:g.213914554C>G	GRCh37
NC_000002.10:g.213622799C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434687.6:c.457G>C MANE Select	ENSP00000412869.1:p.Gly153Arg
ENST00000342002.6:c.475G>C	ENSP00000342876.2:p.Gly159Arg
ENST00000374319.8:c.379G>C	ENSP00000363439.4:p.Gly127Arg
ENST00000374326.7:c.274G>C	ENSP00000363446.3:n.274G>C
ENST00000412444.5:c.610G>C	ENSP00000413680.1:n.610G>C
ENST00000431520.5:c.457G>C	ENSP00000396253.1:p.Gly153Arg
ENST00000434687.5:c.457G>C	ENSP00000412869.1:p.Gly153Arg
ENST00000439848.5:c.636G>C	ENSP00000389548.1:n.636G>C
ENST00000451136.6:c.250G>C	ENSP00000395203.3:p.Gly84Arg
ENST00000453575.5:c.463G>C	ENSP00000411444.1:n.463G>C
ENST00000457361.5:c.250G>C	ENSP00000410447.2:p.Gly84Arg
NM_001079526.1:c.379G>C	NP_001072994.1:p.Gly127Arg
NM_016260.2:c.457G>C	NP_057344.2:p.Gly153Arg
XM_005246384.3:c.457G>C	XP_005246441.1:p.Gly153Arg
XM_005246385.2:c.457G>C	XP_005246442.1:p.Gly153Arg
XM_005246386.3:c.397G>C	XP_005246443.1:p.Gly133Arg
XM_011510801.1:c.478G>C	XP_011509103.1:p.Gly160Arg
XM_011510802.1:c.478G>C	XP_011509104.1:p.Gly160Arg
XM_011510803.1:c.478G>C	XP_011509105.1:p.Gly160Arg
XM_011510804.1:c.478G>C	XP_011509106.1:p.Gly160Arg
XM_011510805.1:c.478G>C	XP_011509107.1:p.Gly160Arg
XM_011510806.1:c.460G>C	XP_011509108.1:p.Gly154Arg
XM_011510807.1:c.460G>C	XP_011509109.1:p.Gly154Arg
XM_011510808.1:c.460G>C	XP_011509110.1:p.Gly154Arg
XM_011510809.1:c.460G>C	XP_011509111.1:p.Gly154Arg
XM_011510810.1:c.460G>C	XP_011509112.1:p.Gly154Arg
XM_011510811.1:c.460G>C	XP_011509113.1:p.Gly154Arg
XM_011510812.1:c.460G>C	XP_011509114.1:p.Gly154Arg
XM_011510813.1:c.475G>C	XP_011509115.1:p.Gly159Arg
XM_011510814.1:c.457G>C	XP_011509116.1:p.Gly153Arg
XM_011510815.1:c.400G>C	XP_011509117.1:p.Gly134Arg
XM_011510816.1:c.385G>C	XP_011509118.1:p.Gly129Arg
XM_011510817.1:c.478G>C	XP_011509119.1:p.Gly160Arg
XM_011510818.1:c.298G>C	XP_011509120.1:p.Gly100Arg
XM_011510819.1:c.397G>C	XP_011509121.1:p.Gly133Arg
XM_005246384.5:c.457G>C	XP_005246441.1:p.Gly153Arg
XM_005246385.4:c.457G>C	XP_005246442.1:p.Gly153Arg
XM_005246386.5:c.397G>C	XP_005246443.1:p.Gly133Arg
XM_011510802.3:c.478G>C	XP_011509104.1:p.Gly160Arg
XM_011510803.3:c.478G>C	XP_011509105.1:p.Gly160Arg
XM_011510804.3:c.478G>C	XP_011509106.1:p.Gly160Arg
XM_011510805.3:c.478G>C	XP_011509107.1:p.Gly160Arg
XM_011510807.3:c.460G>C	XP_011509109.1:p.Gly154Arg
XM_011510808.3:c.460G>C	XP_011509110.1:p.Gly154Arg
XM_011510809.3:c.460G>C	XP_011509111.1:p.Gly154Arg
XM_011510810.3:c.460G>C	XP_011509112.1:p.Gly154Arg
XM_011510811.3:c.460G>C	XP_011509113.1:p.Gly154Arg
XM_011510812.3:c.460G>C	XP_011509114.1:p.Gly154Arg
XM_011510814.3:c.457G>C	XP_011509116.1:p.Gly153Arg
XM_011510815.3:c.400G>C	XP_011509117.1:p.Gly134Arg
XM_011510816.3:c.385G>C	XP_011509118.1:p.Gly129Arg
XM_011510817.3:c.478G>C	XP_011509119.1:p.Gly160Arg
XM_011510818.3:c.298G>C	XP_011509120.1:p.Gly100Arg
XM_011510819.3:c.397G>C	XP_011509121.1:p.Gly133Arg
XM_017003589.2:c.379G>C	XP_016859078.1:p.Gly127Arg
XM_017003590.2:c.379G>C	XP_016859079.1:p.Gly127Arg
XM_017003591.2:c.298G>C	XP_016859080.1:p.Gly100Arg
XM_017003592.2:c.400G>C	XP_016859081.1:p.Gly134Arg
NM_001079526.2:c.379G>C	NP_001072994.1:p.Gly127Arg
NM_001371274.1:c.457G>C	NP_001358203.1:p.Gly153Arg
NM_001371275.1:c.379G>C	NP_001358204.1:p.Gly127Arg
NM_001371276.1:c.379G>C	NP_001358205.1:p.Gly127Arg
NM_001371277.1:c.376G>C	NP_001358206.1:p.Gly126Arg
NM_016260.3:c.457G>C	NP_057344.2:p.Gly153Arg
NM_001387220.1:c.457G>C MANE Select	NP_001374149.1:p.Gly153Arg