Canonical Allele Identifier: CA2354742842

Gene: KIZ

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.21136541C= , CM000682.2:g.21136541C=	GRCh38
NC_000020.10:g.21117182C= , CM000682.1:g.21117182C=	GRCh37
NC_000020.9:g.21065182C=	NCBI36
NG_033122.1:g.15559C=
NG_033122.2:g.15562C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619189.5:c.304C= MANE Select	ENSP00000479542.1:p.Gln102=
ENST00000611685.4:c.167-9024C=
ENST00000616848.4:c.6+4382C=	ENSP00000480612.1:n.6+4382C=
ENST00000619189.4:c.304C=	ENSP00000479542.1:p.Gln102=
ENST00000619574.4:c.169-9024C=	ENSP00000484706.1:n.169-9024C=
ENST00000620553.2:n.360C=
ENST00000620891.4:c.6+4382C=	ENSP00000478019.1:n.6+4382C=
NM_001163022.1:c.6+4382C=	NP_001156494.1:n.6+4382C=
NM_001163023.1:c.6+4382C=	NP_001156495.1:n.6+4382C=
NM_001276389.1:c.169-9024C=	NP_001263318.1:n.169-9024C=
NM_018474.4:c.304C=	NP_060944.3:p.Gln102=
XM_011529296.1:c.304C=	XP_011527598.1:p.Gln102=
XM_011529297.1:c.304C=	XP_011527599.1:p.Gln102=
XM_011529298.1:c.304C=	XP_011527600.1:p.Gln102=
XM_011529299.1:c.6+4382C=	XP_011527601.1:n.6+4382C=
XR_937105.1:n.428C=
NM_001163022.2:c.6+4382C=	NP_001156494.1:n.6+4382C=
NM_001163023.2:c.6+4382C=	NP_001156495.1:n.6+4382C=
NM_001276389.2:c.169-9024C=	NP_001263318.1:n.169-9024C=
NM_001352434.1:c.304C=	NP_001339363.1:p.Gln102=
NM_001352435.1:c.6+4382C=	NP_001339364.1:n.6+4382C=
NM_001352436.1:c.-83C=	NP_001339365.1:n.-83C=
NM_018474.5:c.304C=	NP_060944.3:p.Gln102=
XM_011529296.3:c.304C=	XP_011527598.1:p.Gln102=
XM_011529297.3:c.304C=	XP_011527599.1:p.Gln102=
XM_011529299.3:c.6+4382C=	XP_011527601.1:n.6+4382C=
XM_017027951.2:c.-83C=	XP_016883440.1:n.-83C=
XM_017027952.2:c.6+4382C=	XP_016883441.1:n.6+4382C=
XR_001754334.2:n.370C=
XR_937105.3:n.370C=
NM_018474.6:c.304C= MANE Select	NP_060944.3:p.Gln102=
NM_001163022.3:c.6+4382C=	NP_001156494.1:n.6+4382C=
NM_001163023.3:c.6+4382C=	NP_001156495.1:n.6+4382C=
NM_001352434.2:c.304C=	NP_001339363.1:p.Gln102=
NM_001352435.2:c.6+4382C=	NP_001339364.1:n.6+4382C=
NM_001352436.2:c.-83C=	NP_001339365.1:n.-83C=