Canonical Allele Identifier: CA1990019411
Gene: NOX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89379459_89379482delinsTACTCCACAAACCCAAAGACAAGG , CM000673.2:g.89379459_89379482delinsTACTCCACAAACCCAAAGACAAGG GRCh38
NC_000011.9:g.89112627_89112650delinsTACTCCACAAACCCAAAGACAAGG , CM000673.1:g.89112627_89112650delinsTACTCCACAAACCCAAAGACAAGG GRCh37
NC_000011.8:g.88752275_88752298delinsTACTCCACAAACCCAAAGACAAGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000263317.9:c.1075-5990_1075-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA MANE Select ENSP00000263317.4:n.1075-5990_1075-5967delinsCCTTGTCTTTGGGTTT...
ENST00000263317.8:c.1075-5990_1075-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA ENSP00000263317.4:n.1075-5990_1075-5967delinsCCTTGTCTTTGGGTTT...
ENST00000343727.9:c.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA ENSP00000344747.5:n.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTT...
ENST00000375979.7:c.154-5990_154-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA ENSP00000365146.3:n.154-5990_154-5967delinsCCTTGTCTTTGGGTTTGT...
ENST00000424319.5:c.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA ENSP00000412446.1:n.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTT...
ENST00000525196.5:c.630-39311_630-39288delinsCCTTGTCTTTGGGTTTGTGGAGTA ENSP00000436716.1:n.630-39311_630-39288delinsCCTTGTCTTTGGGTTT...
ENST00000527626.5:c.577-5990_577-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA ENSP00000436093.1:n.577-5990_577-5967delinsCCTTGTCTTTGGGTTTGT...
ENST00000527956.5:c.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA ENSP00000433797.1:n.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTT...
ENST00000528341.5:c.1000-5990_1000-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA ENSP00000436970.1:n.1000-5990_1000-5967delinsCCTTGTCTTTGGGTTT...
ENST00000529343.5:c.630-5990_630-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA ENSP00000435474.1:n.630-5990_630-5967delinsCCTTGTCTTTGGGTTTGT...
ENST00000531342.5:c.154-5990_154-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA ENSP00000435039.1:n.154-5990_154-5967delinsCCTTGTCTTTGGGTTTGT...
ENST00000532825.5:c.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA ENSP00000434924.1:n.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTT...
ENST00000534731.5:c.1075-5990_1075-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA ENSP00000436892.1:n.1075-5990_1075-5967delinsCCTTGTCTTTGGGTTT...
NM_001143836.2:c.1075-5990_1075-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA NP_001137308.1:n.1075-5990_1075-5967delinsCCTTGTCTTTGGGTTTGTG...
NM_001143837.1:c.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA NP_001137309.1:n.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTTGTG...
NM_001291926.1:c.853-5990_853-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA NP_001278855.1:n.853-5990_853-5967delinsCCTTGTCTTTGGGTTTGTGGA...
NM_001291927.1:c.1138-5990_1138-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA NP_001278856.1:n.1138-5990_1138-5967delinsCCTTGTCTTTGGGTTTGTG...
NM_001291929.1:c.1000-5990_1000-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA NP_001278858.1:n.1000-5990_1000-5967delinsCCTTGTCTTTGGGTTTGTG...
NM_001300995.1:c.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA NP_001287924.1:n.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTTGTG...
NM_016931.4:c.1075-5990_1075-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA NP_058627.1:n.1075-5990_1075-5967delinsCCTTGTCTTTGGGTTTGTGGAG...
XM_006718849.2:c.1138-5990_1138-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA XP_006718912.1:n.1138-5990_1138-5967delinsCCTTGTCTTTGGGTTTGTG...
XM_011542857.1:c.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA XP_011541159.1:n.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTTGTG...
XM_011542858.1:c.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA XP_011541160.1:n.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTTGTG...
XM_011542859.1:c.853-5990_853-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA XP_011541161.1:n.853-5990_853-5967delinsCCTTGTCTTTGGGTTTGTGGA...
XM_006718849.4:c.1138-5990_1138-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA XP_006718912.1:n.1138-5990_1138-5967delinsCCTTGTCTTTGGGTTTGTG...
XM_011542857.2:c.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA XP_011541159.1:n.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTTGTG...
XM_017017841.2:c.1057-5990_1057-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA XP_016873330.1:n.1057-5990_1057-5967delinsCCTTGTCTTTGGGTTTGTG...
XM_017017842.1:c.604-5990_604-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA XP_016873331.1:n.604-5990_604-5967delinsCCTTGTCTTTGGGTTTGTGGA...
XM_017017843.2:c.1138-5990_1138-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA XP_016873332.1:n.1138-5990_1138-5967delinsCCTTGTCTTTGGGTTTGTG...
XM_017017844.1:c.577-5990_577-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA XP_016873333.1:n.577-5990_577-5967delinsCCTTGTCTTTGGGTTTGTGGA...
XM_017017845.1:c.577-5990_577-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA XP_016873334.1:n.577-5990_577-5967delinsCCTTGTCTTTGGGTTTGTGGA...
NM_016931.5:c.1075-5990_1075-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA MANE Select NP_058627.2:n.1075-5990_1075-5967delinsCCTTGTCTTTGGGTTTGTGGAG...
NM_001143836.3:c.1075-5990_1075-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA NP_001137308.2:n.1075-5990_1075-5967delinsCCTTGTCTTTGGGTTTGTG...
NM_001143837.2:c.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA NP_001137309.2:n.1003-5990_1003-5967delinsCCTTGTCTTTGGGTTTGTG...
NM_001291926.2:c.853-5990_853-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA NP_001278855.2:n.853-5990_853-5967delinsCCTTGTCTTTGGGTTTGTGGA...
NM_001291929.2:c.1000-5990_1000-5967delinsCCTTGTCTTTGGGTTTGTGGAGTA NP_001278858.2:n.1000-5990_1000-5967delinsCCTTGTCTTTGGGTTTGTG...