Canonical Allele Identifier: CA2652105932

Gene: KIZ

Linked Data

• gnomAD v4: 20-21136597-G-GTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.21136598_21136599insTTT , CM000682.2:g.21136598_21136599insTTT	GRCh38
NC_000020.10:g.21117239_21117240insTTT , CM000682.1:g.21117239_21117240insTTT	GRCh37
NC_000020.9:g.21065239_21065240insTTT	NCBI36
NG_033122.1:g.15616_15617insTTT
NG_033122.2:g.15619_15620insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619189.5:c.315+46_315+47insTTT MANE Select	ENSP00000479542.1:n.315+46_315+47insTTT
ENST00000611685.4:c.167-8967_167-8966insTTT
ENST00000616848.4:c.6+4439_6+4440insTTT	ENSP00000480612.1:n.6+4439_6+4440insTTT
ENST00000619189.4:c.315+46_315+47insTTT	ENSP00000479542.1:n.315+46_315+47insTTT
ENST00000619574.4:c.169-8967_169-8966insTTT	ENSP00000484706.1:n.169-8967_169-8966insTTT
ENST00000620553.2:n.371+46_371+47insTTT
ENST00000620891.4:c.6+4439_6+4440insTTT	ENSP00000478019.1:n.6+4439_6+4440insTTT
NM_001163022.1:c.6+4439_6+4440insTTT	NP_001156494.1:n.6+4439_6+4440insTTT
NM_001163023.1:c.6+4439_6+4440insTTT	NP_001156495.1:n.6+4439_6+4440insTTT
NM_001276389.1:c.169-8967_169-8966insTTT	NP_001263318.1:n.169-8967_169-8966insTTT
NM_018474.4:c.315+46_315+47insTTT	NP_060944.3:n.315+46_315+47insTTT
XM_011529296.1:c.315+46_315+47insTTT	XP_011527598.1:n.315+46_315+47insTTT
XM_011529297.1:c.315+46_315+47insTTT	XP_011527599.1:n.315+46_315+47insTTT
XM_011529298.1:c.315+46_315+47insTTT	XP_011527600.1:n.315+46_315+47insTTT
XM_011529299.1:c.6+4439_6+4440insTTT	XP_011527601.1:n.6+4439_6+4440insTTT
XR_937105.1:n.439+46_439+47insTTT
NM_001163022.2:c.6+4439_6+4440insTTT	NP_001156494.1:n.6+4439_6+4440insTTT
NM_001163023.2:c.6+4439_6+4440insTTT	NP_001156495.1:n.6+4439_6+4440insTTT
NM_001276389.2:c.169-8967_169-8966insTTT	NP_001263318.1:n.169-8967_169-8966insTTT
NM_001352434.1:c.315+46_315+47insTTT	NP_001339363.1:n.315+46_315+47insTTT
NM_001352435.1:c.6+4439_6+4440insTTT	NP_001339364.1:n.6+4439_6+4440insTTT
NM_001352436.1:c.-72+46_-72+47insTTT	NP_001339365.1:n.-72+46_-72+47insTTT
NM_018474.5:c.315+46_315+47insTTT	NP_060944.3:n.315+46_315+47insTTT
XM_011529296.3:c.315+46_315+47insTTT	XP_011527598.1:n.315+46_315+47insTTT
XM_011529297.3:c.315+46_315+47insTTT	XP_011527599.1:n.315+46_315+47insTTT
XM_011529299.3:c.6+4439_6+4440insTTT	XP_011527601.1:n.6+4439_6+4440insTTT
XM_017027951.2:c.-72+46_-72+47insTTT	XP_016883440.1:n.-72+46_-72+47insTTT
XM_017027952.2:c.6+4439_6+4440insTTT	XP_016883441.1:n.6+4439_6+4440insTTT
XR_001754334.2:n.381+46_381+47insTTT
XR_937105.3:n.381+46_381+47insTTT
NM_018474.6:c.315+46_315+47insTTT MANE Select	NP_060944.3:n.315+46_315+47insTTT
NM_001163022.3:c.6+4439_6+4440insTTT	NP_001156494.1:n.6+4439_6+4440insTTT
NM_001163023.3:c.6+4439_6+4440insTTT	NP_001156495.1:n.6+4439_6+4440insTTT
NM_001352434.2:c.315+46_315+47insTTT	NP_001339363.1:n.315+46_315+47insTTT
NM_001352435.2:c.6+4439_6+4440insTTT	NP_001339364.1:n.6+4439_6+4440insTTT
NM_001352436.2:c.-72+46_-72+47insTTT	NP_001339365.1:n.-72+46_-72+47insTTT