Canonical Allele Identifier: CA2815519291

Gene: KIZ

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.21136677_21136678insA , CM000682.2:g.21136677_21136678insA	GRCh38
NC_000020.10:g.21117318_21117319insA , CM000682.1:g.21117318_21117319insA	GRCh37
NC_000020.9:g.21065318_21065319insA	NCBI36
NG_033122.1:g.15695_15696insA
NG_033122.2:g.15698_15699insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619189.5:c.315+125_315+126insA MANE Select	ENSP00000479542.1:n.315+125_315+126insA
ENST00000611685.4:c.167-8888_167-8887insA
ENST00000616848.4:c.6+4518_6+4519insA	ENSP00000480612.1:n.6+4518_6+4519insA
ENST00000619189.4:c.315+125_315+126insA	ENSP00000479542.1:n.315+125_315+126insA
ENST00000619574.4:c.169-8888_169-8887insA	ENSP00000484706.1:n.169-8888_169-8887insA
ENST00000620553.2:n.371+125_371+126insA
ENST00000620891.4:c.6+4518_6+4519insA	ENSP00000478019.1:n.6+4518_6+4519insA
NM_001163022.1:c.6+4518_6+4519insA	NP_001156494.1:n.6+4518_6+4519insA
NM_001163023.1:c.6+4518_6+4519insA	NP_001156495.1:n.6+4518_6+4519insA
NM_001276389.1:c.169-8888_169-8887insA	NP_001263318.1:n.169-8888_169-8887insA
NM_018474.4:c.315+125_315+126insA	NP_060944.3:n.315+125_315+126insA
XM_011529296.1:c.315+125_315+126insA	XP_011527598.1:n.315+125_315+126insA
XM_011529297.1:c.315+125_315+126insA	XP_011527599.1:n.315+125_315+126insA
XM_011529298.1:c.315+125_315+126insA	XP_011527600.1:n.315+125_315+126insA
XM_011529299.1:c.6+4518_6+4519insA	XP_011527601.1:n.6+4518_6+4519insA
XR_937105.1:n.439+125_439+126insA
NM_001163022.2:c.6+4518_6+4519insA	NP_001156494.1:n.6+4518_6+4519insA
NM_001163023.2:c.6+4518_6+4519insA	NP_001156495.1:n.6+4518_6+4519insA
NM_001276389.2:c.169-8888_169-8887insA	NP_001263318.1:n.169-8888_169-8887insA
NM_001352434.1:c.315+125_315+126insA	NP_001339363.1:n.315+125_315+126insA
NM_001352435.1:c.6+4518_6+4519insA	NP_001339364.1:n.6+4518_6+4519insA
NM_001352436.1:c.-72+125_-72+126insA	NP_001339365.1:n.-72+125_-72+126insA
NM_018474.5:c.315+125_315+126insA	NP_060944.3:n.315+125_315+126insA
XM_011529296.3:c.315+125_315+126insA	XP_011527598.1:n.315+125_315+126insA
XM_011529297.3:c.315+125_315+126insA	XP_011527599.1:n.315+125_315+126insA
XM_011529299.3:c.6+4518_6+4519insA	XP_011527601.1:n.6+4518_6+4519insA
XM_017027951.2:c.-72+125_-72+126insA	XP_016883440.1:n.-72+125_-72+126insA
XM_017027952.2:c.6+4518_6+4519insA	XP_016883441.1:n.6+4518_6+4519insA
XR_001754334.2:n.381+125_381+126insA
XR_937105.3:n.381+125_381+126insA
NM_018474.6:c.315+125_315+126insA MANE Select	NP_060944.3:n.315+125_315+126insA
NM_001163022.3:c.6+4518_6+4519insA	NP_001156494.1:n.6+4518_6+4519insA
NM_001163023.3:c.6+4518_6+4519insA	NP_001156495.1:n.6+4518_6+4519insA
NM_001352434.2:c.315+125_315+126insA	NP_001339363.1:n.315+125_315+126insA
NM_001352435.2:c.6+4518_6+4519insA	NP_001339364.1:n.6+4518_6+4519insA
NM_001352436.2:c.-72+125_-72+126insA	NP_001339365.1:n.-72+125_-72+126insA