Canonical Allele Identifier: CA2521715854

Gene: KIZ

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.21136276_21136279del , CM000682.2:g.21136276_21136279del	GRCh38
NC_000020.10:g.21116917_21116920del , CM000682.1:g.21116917_21116920del	GRCh37
NC_000020.9:g.21064917_21064920del	NCBI36
NG_033122.1:g.15294_15297del
NG_033122.2:g.15297_15300del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619189.5:c.153-114_153-111del MANE Select	ENSP00000479542.1:n.153-114_153-111del
ENST00000611685.4:c.167-9289_167-9286del
ENST00000612654.1:c.*61-114_*61-111del	ENSP00000480859.1:n.*61-114_*61-111del
ENST00000616848.4:c.6+4117_6+4120del	ENSP00000480612.1:n.6+4117_6+4120del
ENST00000619189.4:c.153-114_153-111del	ENSP00000479542.1:n.153-114_153-111del
ENST00000619574.4:c.169-9289_169-9286del	ENSP00000484706.1:n.169-9289_169-9286del
ENST00000620553.2:n.209-114_209-111del
ENST00000620891.4:c.6+4117_6+4120del	ENSP00000478019.1:n.6+4117_6+4120del
NM_001163022.1:c.6+4117_6+4120del	NP_001156494.1:n.6+4117_6+4120del
NM_001163023.1:c.6+4117_6+4120del	NP_001156495.1:n.6+4117_6+4120del
NM_001276389.1:c.169-9289_169-9286del	NP_001263318.1:n.169-9289_169-9286del
NM_018474.4:c.153-114_153-111del	NP_060944.3:n.153-114_153-111del
XM_011529296.1:c.153-114_153-111del	XP_011527598.1:n.153-114_153-111del
XM_011529297.1:c.153-114_153-111del	XP_011527599.1:n.153-114_153-111del
XM_011529298.1:c.153-114_153-111del	XP_011527600.1:n.153-114_153-111del
XM_011529299.1:c.6+4117_6+4120del	XP_011527601.1:n.6+4117_6+4120del
XR_937105.1:n.277-114_277-111del
NM_001163022.2:c.6+4117_6+4120del	NP_001156494.1:n.6+4117_6+4120del
NM_001163023.2:c.6+4117_6+4120del	NP_001156495.1:n.6+4117_6+4120del
NM_001276389.2:c.169-9289_169-9286del	NP_001263318.1:n.169-9289_169-9286del
NM_001352434.1:c.153-114_153-111del	NP_001339363.1:n.153-114_153-111del
NM_001352435.1:c.6+4117_6+4120del	NP_001339364.1:n.6+4117_6+4120del
NM_001352436.1:c.-234-114_-234-111del	NP_001339365.1:n.-234-114_-234-111del
NM_018474.5:c.153-114_153-111del	NP_060944.3:n.153-114_153-111del
XM_011529296.3:c.153-114_153-111del	XP_011527598.1:n.153-114_153-111del
XM_011529297.3:c.153-114_153-111del	XP_011527599.1:n.153-114_153-111del
XM_011529299.3:c.6+4117_6+4120del	XP_011527601.1:n.6+4117_6+4120del
XM_017027951.2:c.-234-114_-234-111del	XP_016883440.1:n.-234-114_-234-111del
XM_017027952.2:c.6+4117_6+4120del	XP_016883441.1:n.6+4117_6+4120del
XR_001754334.2:n.219-114_219-111del
XR_937105.3:n.219-114_219-111del
NM_018474.6:c.153-114_153-111del MANE Select	NP_060944.3:n.153-114_153-111del
NM_001163022.3:c.6+4117_6+4120del	NP_001156494.1:n.6+4117_6+4120del
NM_001163023.3:c.6+4117_6+4120del	NP_001156495.1:n.6+4117_6+4120del
NM_001352434.2:c.153-114_153-111del	NP_001339363.1:n.153-114_153-111del
NM_001352435.2:c.6+4117_6+4120del	NP_001339364.1:n.6+4117_6+4120del
NM_001352436.2:c.-234-114_-234-111del	NP_001339365.1:n.-234-114_-234-111del