Canonical Allele Identifier: CA2535763855
Gene: NOX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89379383_89379385del , CM000673.2:g.89379383_89379385del GRCh38
NC_000011.9:g.89112551_89112553del , CM000673.1:g.89112551_89112553del GRCh37
NC_000011.8:g.88752199_88752201del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000263317.9:c.1075-5883_1075-5881del MANE Select ENSP00000263317.4:n.1075-5883_1075-5881de...
ENST00000263317.8:c.1075-5883_1075-5881del ENSP00000263317.4:n.1075-5883_1075-5881de...
ENST00000343727.9:c.1003-5883_1003-5881del ENSP00000344747.5:n.1003-5883_1003-5881de...
ENST00000375979.7:c.154-5883_154-5881del ENSP00000365146.3:n.154-5883_154-5881del
ENST00000424319.5:c.1003-5883_1003-5881del ENSP00000412446.1:n.1003-5883_1003-5881de...
ENST00000525196.5:c.630-39204_630-39202del ENSP00000436716.1:n.630-39204_630-39202de...
ENST00000527626.5:c.577-5883_577-5881del ENSP00000436093.1:n.577-5883_577-5881del
ENST00000527956.5:c.1003-5883_1003-5881del ENSP00000433797.1:n.1003-5883_1003-5881de...
ENST00000528341.5:c.1000-5883_1000-5881del ENSP00000436970.1:n.1000-5883_1000-5881de...
ENST00000529343.5:c.630-5883_630-5881del ENSP00000435474.1:n.630-5883_630-5881del
ENST00000531342.5:c.154-5883_154-5881del ENSP00000435039.1:n.154-5883_154-5881del
ENST00000532825.5:c.1003-5883_1003-5881del ENSP00000434924.1:n.1003-5883_1003-5881de...
ENST00000534731.5:c.1075-5883_1075-5881del ENSP00000436892.1:n.1075-5883_1075-5881de...
NM_001143836.2:c.1075-5883_1075-5881del NP_001137308.1:n.1075-5883_1075-5881del
NM_001143837.1:c.1003-5883_1003-5881del NP_001137309.1:n.1003-5883_1003-5881del
NM_001291926.1:c.853-5883_853-5881del NP_001278855.1:n.853-5883_853-5881del
NM_001291927.1:c.1138-5883_1138-5881del NP_001278856.1:n.1138-5883_1138-5881del
NM_001291929.1:c.1000-5883_1000-5881del NP_001278858.1:n.1000-5883_1000-5881del
NM_001300995.1:c.1003-5883_1003-5881del NP_001287924.1:n.1003-5883_1003-5881del
NM_016931.4:c.1075-5883_1075-5881del NP_058627.1:n.1075-5883_1075-5881del
XM_006718849.2:c.1138-5883_1138-5881del XP_006718912.1:n.1138-5883_1138-5881del
XM_011542857.1:c.1003-5883_1003-5881del XP_011541159.1:n.1003-5883_1003-5881del
XM_011542858.1:c.1003-5883_1003-5881del XP_011541160.1:n.1003-5883_1003-5881del
XM_011542859.1:c.853-5883_853-5881del XP_011541161.1:n.853-5883_853-5881del
XM_006718849.4:c.1138-5883_1138-5881del XP_006718912.1:n.1138-5883_1138-5881del
XM_011542857.2:c.1003-5883_1003-5881del XP_011541159.1:n.1003-5883_1003-5881del
XM_017017841.2:c.1057-5883_1057-5881del XP_016873330.1:n.1057-5883_1057-5881del
XM_017017842.1:c.604-5883_604-5881del XP_016873331.1:n.604-5883_604-5881del
XM_017017843.2:c.1138-5883_1138-5881del XP_016873332.1:n.1138-5883_1138-5881del
XM_017017844.1:c.577-5883_577-5881del XP_016873333.1:n.577-5883_577-5881del
XM_017017845.1:c.577-5883_577-5881del XP_016873334.1:n.577-5883_577-5881del
NM_016931.5:c.1075-5883_1075-5881del MANE Select NP_058627.2:n.1075-5883_1075-5881del
NM_001143836.3:c.1075-5883_1075-5881del NP_001137308.2:n.1075-5883_1075-5881del
NM_001143837.2:c.1003-5883_1003-5881del NP_001137309.2:n.1003-5883_1003-5881del
NM_001291926.2:c.853-5883_853-5881del NP_001278855.2:n.853-5883_853-5881del
NM_001291929.2:c.1000-5883_1000-5881del NP_001278858.2:n.1000-5883_1000-5881del