Canonical Allele Identifier: CA2815519241

Gene: KIZ

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.21136626_21136627insAGAG , CM000682.2:g.21136626_21136627insAGAG	GRCh38
NC_000020.10:g.21117267_21117268insAGAG , CM000682.1:g.21117267_21117268insAGAG	GRCh37
NC_000020.9:g.21065267_21065268insAGAG	NCBI36
NG_033122.1:g.15644_15645insAGAG
NG_033122.2:g.15647_15648insAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619189.5:c.315+74_315+75insAGAG MANE Select	ENSP00000479542.1:n.315+74_315+75insAGAG
ENST00000611685.4:c.167-8939_167-8938insAGAG
ENST00000616848.4:c.6+4467_6+4468insAGAG	ENSP00000480612.1:n.6+4467_6+4468insAGAG
ENST00000619189.4:c.315+74_315+75insAGAG	ENSP00000479542.1:n.315+74_315+75insAGAG
ENST00000619574.4:c.169-8939_169-8938insAGAG	ENSP00000484706.1:n.169-8939_169-8938insAGAG
ENST00000620553.2:n.371+74_371+75insAGAG
ENST00000620891.4:c.6+4467_6+4468insAGAG	ENSP00000478019.1:n.6+4467_6+4468insAGAG
NM_001163022.1:c.6+4467_6+4468insAGAG	NP_001156494.1:n.6+4467_6+4468insAGAG
NM_001163023.1:c.6+4467_6+4468insAGAG	NP_001156495.1:n.6+4467_6+4468insAGAG
NM_001276389.1:c.169-8939_169-8938insAGAG	NP_001263318.1:n.169-8939_169-8938insAGAG
NM_018474.4:c.315+74_315+75insAGAG	NP_060944.3:n.315+74_315+75insAGAG
XM_011529296.1:c.315+74_315+75insAGAG	XP_011527598.1:n.315+74_315+75insAGAG
XM_011529297.1:c.315+74_315+75insAGAG	XP_011527599.1:n.315+74_315+75insAGAG
XM_011529298.1:c.315+74_315+75insAGAG	XP_011527600.1:n.315+74_315+75insAGAG
XM_011529299.1:c.6+4467_6+4468insAGAG	XP_011527601.1:n.6+4467_6+4468insAGAG
XR_937105.1:n.439+74_439+75insAGAG
NM_001163022.2:c.6+4467_6+4468insAGAG	NP_001156494.1:n.6+4467_6+4468insAGAG
NM_001163023.2:c.6+4467_6+4468insAGAG	NP_001156495.1:n.6+4467_6+4468insAGAG
NM_001276389.2:c.169-8939_169-8938insAGAG	NP_001263318.1:n.169-8939_169-8938insAGAG
NM_001352434.1:c.315+74_315+75insAGAG	NP_001339363.1:n.315+74_315+75insAGAG
NM_001352435.1:c.6+4467_6+4468insAGAG	NP_001339364.1:n.6+4467_6+4468insAGAG
NM_001352436.1:c.-72+74_-72+75insAGAG	NP_001339365.1:n.-72+74_-72+75insAGAG
NM_018474.5:c.315+74_315+75insAGAG	NP_060944.3:n.315+74_315+75insAGAG
XM_011529296.3:c.315+74_315+75insAGAG	XP_011527598.1:n.315+74_315+75insAGAG
XM_011529297.3:c.315+74_315+75insAGAG	XP_011527599.1:n.315+74_315+75insAGAG
XM_011529299.3:c.6+4467_6+4468insAGAG	XP_011527601.1:n.6+4467_6+4468insAGAG
XM_017027951.2:c.-72+74_-72+75insAGAG	XP_016883440.1:n.-72+74_-72+75insAGAG
XM_017027952.2:c.6+4467_6+4468insAGAG	XP_016883441.1:n.6+4467_6+4468insAGAG
XR_001754334.2:n.381+74_381+75insAGAG
XR_937105.3:n.381+74_381+75insAGAG
NM_018474.6:c.315+74_315+75insAGAG MANE Select	NP_060944.3:n.315+74_315+75insAGAG
NM_001163022.3:c.6+4467_6+4468insAGAG	NP_001156494.1:n.6+4467_6+4468insAGAG
NM_001163023.3:c.6+4467_6+4468insAGAG	NP_001156495.1:n.6+4467_6+4468insAGAG
NM_001352434.2:c.315+74_315+75insAGAG	NP_001339363.1:n.315+74_315+75insAGAG
NM_001352435.2:c.6+4467_6+4468insAGAG	NP_001339364.1:n.6+4467_6+4468insAGAG
NM_001352436.2:c.-72+74_-72+75insAGAG	NP_001339365.1:n.-72+74_-72+75insAGAG