Canonical Allele Identifier: CA940660342

Gene: NOX4

Linked Data

• dbSNP Id: rs1940111726
• gnomAD v3: 11-89379459-TACTCCACAAACCCAAAGACAAGG-T
• gnomAD v4: 11-89379459-TACTCCACAAACCCAAAGACAAGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89379461_89379483del , CM000673.2:g.89379461_89379483del	GRCh38
NC_000011.9:g.89112629_89112651del , CM000673.1:g.89112629_89112651del	GRCh37
NC_000011.8:g.88752277_88752299del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263317.9:c.1075-5990_1075-5968del MANE Select	ENSP00000263317.4:n.1075-5990_1075-5968del
ENST00000263317.8:c.1075-5990_1075-5968del	ENSP00000263317.4:n.1075-5990_1075-5968del
ENST00000343727.9:c.1003-5990_1003-5968del	ENSP00000344747.5:n.1003-5990_1003-5968del
ENST00000375979.7:c.154-5990_154-5968del	ENSP00000365146.3:n.154-5990_154-5968del
ENST00000424319.5:c.1003-5990_1003-5968del	ENSP00000412446.1:n.1003-5990_1003-5968del
ENST00000525196.5:c.630-39311_630-39289del	ENSP00000436716.1:n.630-39311_630-39289del
ENST00000527626.5:c.577-5990_577-5968del	ENSP00000436093.1:n.577-5990_577-5968del
ENST00000527956.5:c.1003-5990_1003-5968del	ENSP00000433797.1:n.1003-5990_1003-5968del
ENST00000528341.5:c.1000-5990_1000-5968del	ENSP00000436970.1:n.1000-5990_1000-5968del
ENST00000529343.5:c.630-5990_630-5968del	ENSP00000435474.1:n.630-5990_630-5968del
ENST00000531342.5:c.154-5990_154-5968del	ENSP00000435039.1:n.154-5990_154-5968del
ENST00000532825.5:c.1003-5990_1003-5968del	ENSP00000434924.1:n.1003-5990_1003-5968del
ENST00000534731.5:c.1075-5990_1075-5968del	ENSP00000436892.1:n.1075-5990_1075-5968del
NM_001143836.2:c.1075-5990_1075-5968del	NP_001137308.1:n.1075-5990_1075-5968del
NM_001143837.1:c.1003-5990_1003-5968del	NP_001137309.1:n.1003-5990_1003-5968del
NM_001291926.1:c.853-5990_853-5968del	NP_001278855.1:n.853-5990_853-5968del
NM_001291927.1:c.1138-5990_1138-5968del	NP_001278856.1:n.1138-5990_1138-5968del
NM_001291929.1:c.1000-5990_1000-5968del	NP_001278858.1:n.1000-5990_1000-5968del
NM_001300995.1:c.1003-5990_1003-5968del	NP_001287924.1:n.1003-5990_1003-5968del
NM_016931.4:c.1075-5990_1075-5968del	NP_058627.1:n.1075-5990_1075-5968del
XM_006718849.2:c.1138-5990_1138-5968del	XP_006718912.1:n.1138-5990_1138-5968del
XM_011542857.1:c.1003-5990_1003-5968del	XP_011541159.1:n.1003-5990_1003-5968del
XM_011542858.1:c.1003-5990_1003-5968del	XP_011541160.1:n.1003-5990_1003-5968del
XM_011542859.1:c.853-5990_853-5968del	XP_011541161.1:n.853-5990_853-5968del
XM_006718849.4:c.1138-5990_1138-5968del	XP_006718912.1:n.1138-5990_1138-5968del
XM_011542857.2:c.1003-5990_1003-5968del	XP_011541159.1:n.1003-5990_1003-5968del
XM_017017841.2:c.1057-5990_1057-5968del	XP_016873330.1:n.1057-5990_1057-5968del
XM_017017842.1:c.604-5990_604-5968del	XP_016873331.1:n.604-5990_604-5968del
XM_017017843.2:c.1138-5990_1138-5968del	XP_016873332.1:n.1138-5990_1138-5968del
XM_017017844.1:c.577-5990_577-5968del	XP_016873333.1:n.577-5990_577-5968del
XM_017017845.1:c.577-5990_577-5968del	XP_016873334.1:n.577-5990_577-5968del
NM_016931.5:c.1075-5990_1075-5968del MANE Select	NP_058627.2:n.1075-5990_1075-5968del
NM_001143836.3:c.1075-5990_1075-5968del	NP_001137308.2:n.1075-5990_1075-5968del
NM_001143837.2:c.1003-5990_1003-5968del	NP_001137309.2:n.1003-5990_1003-5968del
NM_001291926.2:c.853-5990_853-5968del	NP_001278855.2:n.853-5990_853-5968del
NM_001291929.2:c.1000-5990_1000-5968del	NP_001278858.2:n.1000-5990_1000-5968del