Canonical Allele Identifier: CA2354742679

Gene: KIZ

Linked Data

• dbSNP Id: rs2032173784

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.21136167_21136168del , CM000682.2:g.21136167_21136168del	GRCh38
NC_000020.10:g.21116808_21116809del , CM000682.1:g.21116808_21116809del	GRCh37
NC_000020.9:g.21064808_21064809del	NCBI36
NG_033122.1:g.15185_15186del
NG_033122.2:g.15188_15189del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619189.5:c.153-223_153-222del MANE Select	ENSP00000479542.1:n.153-223_153-222del
ENST00000611685.4:c.167-9398_167-9397del
ENST00000612654.1:c.*61-223_*61-222del	ENSP00000480859.1:n.*61-223_*61-222del
ENST00000616848.4:c.6+4008_6+4009del	ENSP00000480612.1:n.6+4008_6+4009del
ENST00000619189.4:c.153-223_153-222del	ENSP00000479542.1:n.153-223_153-222del
ENST00000619574.4:c.169-9398_169-9397del	ENSP00000484706.1:n.169-9398_169-9397del
ENST00000620553.2:n.209-223_209-222del
ENST00000620891.4:c.6+4008_6+4009del	ENSP00000478019.1:n.6+4008_6+4009del
NM_001163022.1:c.6+4008_6+4009del	NP_001156494.1:n.6+4008_6+4009del
NM_001163023.1:c.6+4008_6+4009del	NP_001156495.1:n.6+4008_6+4009del
NM_001276389.1:c.169-9398_169-9397del	NP_001263318.1:n.169-9398_169-9397del
NM_018474.4:c.153-223_153-222del	NP_060944.3:n.153-223_153-222del
XM_011529296.1:c.153-223_153-222del	XP_011527598.1:n.153-223_153-222del
XM_011529297.1:c.153-223_153-222del	XP_011527599.1:n.153-223_153-222del
XM_011529298.1:c.153-223_153-222del	XP_011527600.1:n.153-223_153-222del
XM_011529299.1:c.6+4008_6+4009del	XP_011527601.1:n.6+4008_6+4009del
XR_937105.1:n.277-223_277-222del
NM_001163022.2:c.6+4008_6+4009del	NP_001156494.1:n.6+4008_6+4009del
NM_001163023.2:c.6+4008_6+4009del	NP_001156495.1:n.6+4008_6+4009del
NM_001276389.2:c.169-9398_169-9397del	NP_001263318.1:n.169-9398_169-9397del
NM_001352434.1:c.153-223_153-222del	NP_001339363.1:n.153-223_153-222del
NM_001352435.1:c.6+4008_6+4009del	NP_001339364.1:n.6+4008_6+4009del
NM_001352436.1:c.-234-223_-234-222del	NP_001339365.1:n.-234-223_-234-222del
NM_018474.5:c.153-223_153-222del	NP_060944.3:n.153-223_153-222del
XM_011529296.3:c.153-223_153-222del	XP_011527598.1:n.153-223_153-222del
XM_011529297.3:c.153-223_153-222del	XP_011527599.1:n.153-223_153-222del
XM_011529299.3:c.6+4008_6+4009del	XP_011527601.1:n.6+4008_6+4009del
XM_017027951.2:c.-234-223_-234-222del	XP_016883440.1:n.-234-223_-234-222del
XM_017027952.2:c.6+4008_6+4009del	XP_016883441.1:n.6+4008_6+4009del
XR_001754334.2:n.219-223_219-222del
XR_937105.3:n.219-223_219-222del
NM_018474.6:c.153-223_153-222del MANE Select	NP_060944.3:n.153-223_153-222del
NM_001163022.3:c.6+4008_6+4009del	NP_001156494.1:n.6+4008_6+4009del
NM_001163023.3:c.6+4008_6+4009del	NP_001156495.1:n.6+4008_6+4009del
NM_001352434.2:c.153-223_153-222del	NP_001339363.1:n.153-223_153-222del
NM_001352435.2:c.6+4008_6+4009del	NP_001339364.1:n.6+4008_6+4009del
NM_001352436.2:c.-234-223_-234-222del	NP_001339365.1:n.-234-223_-234-222del