Canonical Allele Identifier: CA1990064102

Gene: NOX4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89468459G= , CM000673.2:g.89468459G=	GRCh38
NC_000011.9:g.89201627G= , CM000673.1:g.89201627G=	GRCh37
NC_000011.8:g.88841275G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016931.5:c.154-16564C= MANE Select	NP_058627.2:n.154-16564C=
ENST00000263317.9:c.154-16564C= MANE Select	ENSP00000263317.4:n.154-16564C=
NM_001143836.2:c.154-16564C=	NP_001137308.1:n.154-16564C=
NM_001143836.3:c.154-16564C=	NP_001137308.2:n.154-16564C=
NM_001143837.1:c.82-16564C=	NP_001137309.1:n.82-16564C=
NM_001143837.2:c.82-16564C=	NP_001137309.2:n.82-16564C=
NM_001291926.1:c.-65-16568C=	NP_001278855.1:n.-65-16568C=
NM_001291926.2:c.-65-16568C=	NP_001278855.2:n.-65-16568C=
NM_001291927.1:c.217-16564C=	NP_001278856.1:n.217-16564C=
NM_001291929.1:c.79-16564C=	NP_001278858.1:n.79-16564C=
NM_001291929.2:c.79-16564C=	NP_001278858.2:n.79-16564C=
NM_001300995.1:c.82-16564C=	NP_001287924.1:n.82-16564C=
NM_016931.4:c.154-16564C=	NP_058627.1:n.154-16564C=
ENST00000263317.8:c.154-16564C=	ENSP00000263317.4:n.154-16564C=
ENST00000343727.9:c.82-16564C=	ENSP00000344747.5:n.82-16564C=
ENST00000375979.7:c.153+21999C=	ENSP00000365146.3:n.153+21999C=
ENST00000424319.5:c.82-16564C=	ENSP00000412446.1:n.82-16564C=
ENST00000525196.5:c.154-16564C=	ENSP00000436716.1:n.154-16564C=
ENST00000525278.1:n.302-16564C=
ENST00000527626.5:c.-24+21999C=	ENSP00000436093.1:n.-24+21999C=
ENST00000527956.5:c.82-16564C=	ENSP00000433797.1:n.82-16564C=
ENST00000528341.5:c.79-16564C=	ENSP00000436970.1:n.79-16564C=
ENST00000529343.5:c.154-16564C=	ENSP00000435474.1:n.154-16564C=
ENST00000531342.5:c.153+21999C=	ENSP00000435039.1:n.153+21999C=
ENST00000532825.5:c.82-16564C=	ENSP00000434924.1:n.82-16564C=
ENST00000534731.5:c.154-16564C=	ENSP00000436892.1:n.154-16564C=
XM_006718849.2:c.217-16564C=	XP_006718912.1:n.217-16564C=
XM_006718849.4:c.217-16564C=	XP_006718912.1:n.217-16564C=
XM_011542857.1:c.82-16564C=	XP_011541159.1:n.82-16564C=
XM_011542857.2:c.82-16564C=	XP_011541159.1:n.82-16564C=
XM_011542858.1:c.82-16564C=	XP_011541160.1:n.82-16564C=
XM_011542859.1:c.-65-16568C=	XP_011541161.1:n.-65-16568C=
XM_017017841.2:c.217-16564C=	XP_016873330.1:n.217-16564C=
XM_017017843.2:c.217-16564C=	XP_016873332.1:n.217-16564C=
XM_017017844.1:c.-439-16568C=	XP_016873333.1:n.-439-16568C=