Canonical Allele Identifier: CA2815519195

Gene: KIZ

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.21136554_21136555insAG , CM000682.2:g.21136554_21136555insAG	GRCh38
NC_000020.10:g.21117195_21117196insAG , CM000682.1:g.21117195_21117196insAG	GRCh37
NC_000020.9:g.21065195_21065196insAG	NCBI36
NG_033122.1:g.15572_15573insAG
NG_033122.2:g.15575_15576insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619189.5:c.315+2_315+3insAG MANE Select	ENSP00000479542.1:n.315+2_315+3insAG
ENST00000611685.4:c.167-9011_167-9010insAG
ENST00000616848.4:c.6+4395_6+4396insAG	ENSP00000480612.1:n.6+4395_6+4396insAG
ENST00000619189.4:c.315+2_315+3insAG	ENSP00000479542.1:n.315+2_315+3insAG
ENST00000619574.4:c.169-9011_169-9010insAG	ENSP00000484706.1:n.169-9011_169-9010insAG
ENST00000620553.2:n.371+2_371+3insAG
ENST00000620891.4:c.6+4395_6+4396insAG	ENSP00000478019.1:n.6+4395_6+4396insAG
NM_001163022.1:c.6+4395_6+4396insAG	NP_001156494.1:n.6+4395_6+4396insAG
NM_001163023.1:c.6+4395_6+4396insAG	NP_001156495.1:n.6+4395_6+4396insAG
NM_001276389.1:c.169-9011_169-9010insAG	NP_001263318.1:n.169-9011_169-9010insAG
NM_018474.4:c.315+2_315+3insAG	NP_060944.3:n.315+2_315+3insAG
XM_011529296.1:c.315+2_315+3insAG	XP_011527598.1:n.315+2_315+3insAG
XM_011529297.1:c.315+2_315+3insAG	XP_011527599.1:n.315+2_315+3insAG
XM_011529298.1:c.315+2_315+3insAG	XP_011527600.1:n.315+2_315+3insAG
XM_011529299.1:c.6+4395_6+4396insAG	XP_011527601.1:n.6+4395_6+4396insAG
XR_937105.1:n.439+2_439+3insAG
NM_001163022.2:c.6+4395_6+4396insAG	NP_001156494.1:n.6+4395_6+4396insAG
NM_001163023.2:c.6+4395_6+4396insAG	NP_001156495.1:n.6+4395_6+4396insAG
NM_001276389.2:c.169-9011_169-9010insAG	NP_001263318.1:n.169-9011_169-9010insAG
NM_001352434.1:c.315+2_315+3insAG	NP_001339363.1:n.315+2_315+3insAG
NM_001352435.1:c.6+4395_6+4396insAG	NP_001339364.1:n.6+4395_6+4396insAG
NM_001352436.1:c.-72+2_-72+3insAG	NP_001339365.1:n.-72+2_-72+3insAG
NM_018474.5:c.315+2_315+3insAG	NP_060944.3:n.315+2_315+3insAG
XM_011529296.3:c.315+2_315+3insAG	XP_011527598.1:n.315+2_315+3insAG
XM_011529297.3:c.315+2_315+3insAG	XP_011527599.1:n.315+2_315+3insAG
XM_011529299.3:c.6+4395_6+4396insAG	XP_011527601.1:n.6+4395_6+4396insAG
XM_017027951.2:c.-72+2_-72+3insAG	XP_016883440.1:n.-72+2_-72+3insAG
XM_017027952.2:c.6+4395_6+4396insAG	XP_016883441.1:n.6+4395_6+4396insAG
XR_001754334.2:n.381+2_381+3insAG
XR_937105.3:n.381+2_381+3insAG
NM_018474.6:c.315+2_315+3insAG MANE Select	NP_060944.3:n.315+2_315+3insAG
NM_001163022.3:c.6+4395_6+4396insAG	NP_001156494.1:n.6+4395_6+4396insAG
NM_001163023.3:c.6+4395_6+4396insAG	NP_001156495.1:n.6+4395_6+4396insAG
NM_001352434.2:c.315+2_315+3insAG	NP_001339363.1:n.315+2_315+3insAG
NM_001352435.2:c.6+4395_6+4396insAG	NP_001339364.1:n.6+4395_6+4396insAG
NM_001352436.2:c.-72+2_-72+3insAG	NP_001339365.1:n.-72+2_-72+3insAG