Canonical Allele Identifier: CA2354742853

Gene: KIZ

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.21136573_21136574delinsGT , CM000682.2:g.21136573_21136574delinsGT	GRCh38
NC_000020.10:g.21117214_21117215delinsGT , CM000682.1:g.21117214_21117215delinsGT	GRCh37
NC_000020.9:g.21065214_21065215delinsGT	NCBI36
NG_033122.1:g.15591_15592delinsGT
NG_033122.2:g.15594_15595delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619189.5:c.315+21_315+22delinsGT MANE Select	ENSP00000479542.1:n.315+21_315+22delinsGT
ENST00000611685.4:c.167-8992_167-8991delinsGT
ENST00000616848.4:c.6+4414_6+4415delinsGT	ENSP00000480612.1:n.6+4414_6+4415delinsGT
ENST00000619189.4:c.315+21_315+22delinsGT	ENSP00000479542.1:n.315+21_315+22delinsGT
ENST00000619574.4:c.169-8992_169-8991delinsGT	ENSP00000484706.1:n.169-8992_169-8991delinsGT
ENST00000620553.2:n.371+21_371+22delinsGT
ENST00000620891.4:c.6+4414_6+4415delinsGT	ENSP00000478019.1:n.6+4414_6+4415delinsGT
NM_001163022.1:c.6+4414_6+4415delinsGT	NP_001156494.1:n.6+4414_6+4415delinsGT
NM_001163023.1:c.6+4414_6+4415delinsGT	NP_001156495.1:n.6+4414_6+4415delinsGT
NM_001276389.1:c.169-8992_169-8991delinsGT	NP_001263318.1:n.169-8992_169-8991delinsGT
NM_018474.4:c.315+21_315+22delinsGT	NP_060944.3:n.315+21_315+22delinsGT
XM_011529296.1:c.315+21_315+22delinsGT	XP_011527598.1:n.315+21_315+22delinsGT
XM_011529297.1:c.315+21_315+22delinsGT	XP_011527599.1:n.315+21_315+22delinsGT
XM_011529298.1:c.315+21_315+22delinsGT	XP_011527600.1:n.315+21_315+22delinsGT
XM_011529299.1:c.6+4414_6+4415delinsGT	XP_011527601.1:n.6+4414_6+4415delinsGT
XR_937105.1:n.439+21_439+22delinsGT
NM_001163022.2:c.6+4414_6+4415delinsGT	NP_001156494.1:n.6+4414_6+4415delinsGT
NM_001163023.2:c.6+4414_6+4415delinsGT	NP_001156495.1:n.6+4414_6+4415delinsGT
NM_001276389.2:c.169-8992_169-8991delinsGT	NP_001263318.1:n.169-8992_169-8991delinsGT
NM_001352434.1:c.315+21_315+22delinsGT	NP_001339363.1:n.315+21_315+22delinsGT
NM_001352435.1:c.6+4414_6+4415delinsGT	NP_001339364.1:n.6+4414_6+4415delinsGT
NM_001352436.1:c.-72+21_-72+22delinsGT	NP_001339365.1:n.-72+21_-72+22delinsGT
NM_018474.5:c.315+21_315+22delinsGT	NP_060944.3:n.315+21_315+22delinsGT
XM_011529296.3:c.315+21_315+22delinsGT	XP_011527598.1:n.315+21_315+22delinsGT
XM_011529297.3:c.315+21_315+22delinsGT	XP_011527599.1:n.315+21_315+22delinsGT
XM_011529299.3:c.6+4414_6+4415delinsGT	XP_011527601.1:n.6+4414_6+4415delinsGT
XM_017027951.2:c.-72+21_-72+22delinsGT	XP_016883440.1:n.-72+21_-72+22delinsGT
XM_017027952.2:c.6+4414_6+4415delinsGT	XP_016883441.1:n.6+4414_6+4415delinsGT
XR_001754334.2:n.381+21_381+22delinsGT
XR_937105.3:n.381+21_381+22delinsGT
NM_018474.6:c.315+21_315+22delinsGT MANE Select	NP_060944.3:n.315+21_315+22delinsGT
NM_001163022.3:c.6+4414_6+4415delinsGT	NP_001156494.1:n.6+4414_6+4415delinsGT
NM_001163023.3:c.6+4414_6+4415delinsGT	NP_001156495.1:n.6+4414_6+4415delinsGT
NM_001352434.2:c.315+21_315+22delinsGT	NP_001339363.1:n.315+21_315+22delinsGT
NM_001352435.2:c.6+4414_6+4415delinsGT	NP_001339364.1:n.6+4414_6+4415delinsGT
NM_001352436.2:c.-72+21_-72+22delinsGT	NP_001339365.1:n.-72+21_-72+22delinsGT