Canonical Allele Identifier: CA2815519280

Gene: KIZ

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.21136651_21136652insAC , CM000682.2:g.21136651_21136652insAC	GRCh38
NC_000020.10:g.21117292_21117293insAC , CM000682.1:g.21117292_21117293insAC	GRCh37
NC_000020.9:g.21065292_21065293insAC	NCBI36
NG_033122.1:g.15669_15670insAC
NG_033122.2:g.15672_15673insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619189.5:c.315+99_315+100insAC MANE Select	ENSP00000479542.1:n.315+99_315+100insAC
ENST00000611685.4:c.167-8914_167-8913insAC
ENST00000616848.4:c.6+4492_6+4493insAC	ENSP00000480612.1:n.6+4492_6+4493insAC
ENST00000619189.4:c.315+99_315+100insAC	ENSP00000479542.1:n.315+99_315+100insAC
ENST00000619574.4:c.169-8914_169-8913insAC	ENSP00000484706.1:n.169-8914_169-8913insAC
ENST00000620553.2:n.371+99_371+100insAC
ENST00000620891.4:c.6+4492_6+4493insAC	ENSP00000478019.1:n.6+4492_6+4493insAC
NM_001163022.1:c.6+4492_6+4493insAC	NP_001156494.1:n.6+4492_6+4493insAC
NM_001163023.1:c.6+4492_6+4493insAC	NP_001156495.1:n.6+4492_6+4493insAC
NM_001276389.1:c.169-8914_169-8913insAC	NP_001263318.1:n.169-8914_169-8913insAC
NM_018474.4:c.315+99_315+100insAC	NP_060944.3:n.315+99_315+100insAC
XM_011529296.1:c.315+99_315+100insAC	XP_011527598.1:n.315+99_315+100insAC
XM_011529297.1:c.315+99_315+100insAC	XP_011527599.1:n.315+99_315+100insAC
XM_011529298.1:c.315+99_315+100insAC	XP_011527600.1:n.315+99_315+100insAC
XM_011529299.1:c.6+4492_6+4493insAC	XP_011527601.1:n.6+4492_6+4493insAC
XR_937105.1:n.439+99_439+100insAC
NM_001163022.2:c.6+4492_6+4493insAC	NP_001156494.1:n.6+4492_6+4493insAC
NM_001163023.2:c.6+4492_6+4493insAC	NP_001156495.1:n.6+4492_6+4493insAC
NM_001276389.2:c.169-8914_169-8913insAC	NP_001263318.1:n.169-8914_169-8913insAC
NM_001352434.1:c.315+99_315+100insAC	NP_001339363.1:n.315+99_315+100insAC
NM_001352435.1:c.6+4492_6+4493insAC	NP_001339364.1:n.6+4492_6+4493insAC
NM_001352436.1:c.-72+99_-72+100insAC	NP_001339365.1:n.-72+99_-72+100insAC
NM_018474.5:c.315+99_315+100insAC	NP_060944.3:n.315+99_315+100insAC
XM_011529296.3:c.315+99_315+100insAC	XP_011527598.1:n.315+99_315+100insAC
XM_011529297.3:c.315+99_315+100insAC	XP_011527599.1:n.315+99_315+100insAC
XM_011529299.3:c.6+4492_6+4493insAC	XP_011527601.1:n.6+4492_6+4493insAC
XM_017027951.2:c.-72+99_-72+100insAC	XP_016883440.1:n.-72+99_-72+100insAC
XM_017027952.2:c.6+4492_6+4493insAC	XP_016883441.1:n.6+4492_6+4493insAC
XR_001754334.2:n.381+99_381+100insAC
XR_937105.3:n.381+99_381+100insAC
NM_018474.6:c.315+99_315+100insAC MANE Select	NP_060944.3:n.315+99_315+100insAC
NM_001163022.3:c.6+4492_6+4493insAC	NP_001156494.1:n.6+4492_6+4493insAC
NM_001163023.3:c.6+4492_6+4493insAC	NP_001156495.1:n.6+4492_6+4493insAC
NM_001352434.2:c.315+99_315+100insAC	NP_001339363.1:n.315+99_315+100insAC
NM_001352435.2:c.6+4492_6+4493insAC	NP_001339364.1:n.6+4492_6+4493insAC
NM_001352436.2:c.-72+99_-72+100insAC	NP_001339365.1:n.-72+99_-72+100insAC