Canonical Allele Identifier: CA2652105982

Gene: KIZ

Linked Data

• gnomAD v4: 20-21136620-ATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.21136621_21136622del , CM000682.2:g.21136621_21136622del	GRCh38
NC_000020.10:g.21117262_21117263del , CM000682.1:g.21117262_21117263del	GRCh37
NC_000020.9:g.21065262_21065263del	NCBI36
NG_033122.1:g.15639_15640del
NG_033122.2:g.15642_15643del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619189.5:c.315+69_315+70del MANE Select	ENSP00000479542.1:n.315+69_315+70del
ENST00000611685.4:c.167-8944_167-8943del
ENST00000616848.4:c.6+4462_6+4463del	ENSP00000480612.1:n.6+4462_6+4463del
ENST00000619189.4:c.315+69_315+70del	ENSP00000479542.1:n.315+69_315+70del
ENST00000619574.4:c.169-8944_169-8943del	ENSP00000484706.1:n.169-8944_169-8943del
ENST00000620553.2:n.371+69_371+70del
ENST00000620891.4:c.6+4462_6+4463del	ENSP00000478019.1:n.6+4462_6+4463del
NM_001163022.1:c.6+4462_6+4463del	NP_001156494.1:n.6+4462_6+4463del
NM_001163023.1:c.6+4462_6+4463del	NP_001156495.1:n.6+4462_6+4463del
NM_001276389.1:c.169-8944_169-8943del	NP_001263318.1:n.169-8944_169-8943del
NM_018474.4:c.315+69_315+70del	NP_060944.3:n.315+69_315+70del
XM_011529296.1:c.315+69_315+70del	XP_011527598.1:n.315+69_315+70del
XM_011529297.1:c.315+69_315+70del	XP_011527599.1:n.315+69_315+70del
XM_011529298.1:c.315+69_315+70del	XP_011527600.1:n.315+69_315+70del
XM_011529299.1:c.6+4462_6+4463del	XP_011527601.1:n.6+4462_6+4463del
XR_937105.1:n.439+69_439+70del
NM_001163022.2:c.6+4462_6+4463del	NP_001156494.1:n.6+4462_6+4463del
NM_001163023.2:c.6+4462_6+4463del	NP_001156495.1:n.6+4462_6+4463del
NM_001276389.2:c.169-8944_169-8943del	NP_001263318.1:n.169-8944_169-8943del
NM_001352434.1:c.315+69_315+70del	NP_001339363.1:n.315+69_315+70del
NM_001352435.1:c.6+4462_6+4463del	NP_001339364.1:n.6+4462_6+4463del
NM_001352436.1:c.-72+69_-72+70del	NP_001339365.1:n.-72+69_-72+70del
NM_018474.5:c.315+69_315+70del	NP_060944.3:n.315+69_315+70del
XM_011529296.3:c.315+69_315+70del	XP_011527598.1:n.315+69_315+70del
XM_011529297.3:c.315+69_315+70del	XP_011527599.1:n.315+69_315+70del
XM_011529299.3:c.6+4462_6+4463del	XP_011527601.1:n.6+4462_6+4463del
XM_017027951.2:c.-72+69_-72+70del	XP_016883440.1:n.-72+69_-72+70del
XM_017027952.2:c.6+4462_6+4463del	XP_016883441.1:n.6+4462_6+4463del
XR_001754334.2:n.381+69_381+70del
XR_937105.3:n.381+69_381+70del
NM_018474.6:c.315+69_315+70del MANE Select	NP_060944.3:n.315+69_315+70del
NM_001163022.3:c.6+4462_6+4463del	NP_001156494.1:n.6+4462_6+4463del
NM_001163023.3:c.6+4462_6+4463del	NP_001156495.1:n.6+4462_6+4463del
NM_001352434.2:c.315+69_315+70del	NP_001339363.1:n.315+69_315+70del
NM_001352435.2:c.6+4462_6+4463del	NP_001339364.1:n.6+4462_6+4463del
NM_001352436.2:c.-72+69_-72+70del	NP_001339365.1:n.-72+69_-72+70del