Canonical Allele Identifier: CA13446464

Gene: NOX4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89473343T>C , CM000673.2:g.89473343T>C	GRCh38
NC_000011.9:g.89206511T>C , CM000673.1:g.89206511T>C	GRCh37
NC_000011.8:g.88846159T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263317.9:c.153+17115A>G MANE Select	ENSP00000263317.4:n.153+17115A>G
ENST00000263317.8:c.153+17115A>G	ENSP00000263317.4:n.153+17115A>G
ENST00000343727.9:c.81+17115A>G	ENSP00000344747.5:n.81+17115A>G
ENST00000375979.7:c.153+17115A>G	ENSP00000365146.3:n.153+17115A>G
ENST00000424319.5:c.81+17115A>G	ENSP00000412446.1:n.81+17115A>G
ENST00000525196.5:c.153+17115A>G	ENSP00000436716.1:n.153+17115A>G
ENST00000525278.1:n.301+17115A>G
ENST00000527626.5:c.-24+17115A>G	ENSP00000436093.1:n.-24+17115A>G
ENST00000527956.5:c.81+17115A>G	ENSP00000433797.1:n.81+17115A>G
ENST00000528341.5:c.78+17264A>G	ENSP00000436970.1:n.78+17264A>G
ENST00000529343.5:c.153+17115A>G	ENSP00000435474.1:n.153+17115A>G
ENST00000531342.5:c.153+17115A>G	ENSP00000435039.1:n.153+17115A>G
ENST00000532825.5:c.81+17115A>G	ENSP00000434924.1:n.81+17115A>G
ENST00000534731.5:c.153+17115A>G	ENSP00000436892.1:n.153+17115A>G
NM_001143836.2:c.153+17115A>G	NP_001137308.1:n.153+17115A>G
NM_001143837.1:c.81+17115A>G	NP_001137309.1:n.81+17115A>G
NM_001291926.1:c.-66+17115A>G	NP_001278855.1:n.-66+17115A>G
NM_001291927.1:c.216+17115A>G	NP_001278856.1:n.216+17115A>G
NM_001291929.1:c.78+17264A>G	NP_001278858.1:n.78+17264A>G
NM_001300995.1:c.81+17115A>G	NP_001287924.1:n.81+17115A>G
NM_016931.4:c.153+17115A>G	NP_058627.1:n.153+17115A>G
XM_006718849.2:c.216+17115A>G	XP_006718912.1:n.216+17115A>G
XM_011542857.1:c.81+17115A>G	XP_011541159.1:n.81+17115A>G
XM_011542858.1:c.81+17115A>G	XP_011541160.1:n.81+17115A>G
XM_011542859.1:c.-66+17264A>G	XP_011541161.1:n.-66+17264A>G
XM_006718849.4:c.216+17115A>G	XP_006718912.1:n.216+17115A>G
XM_011542857.2:c.81+17115A>G	XP_011541159.1:n.81+17115A>G
XM_017017841.2:c.216+17115A>G	XP_016873330.1:n.216+17115A>G
XM_017017843.2:c.216+17115A>G	XP_016873332.1:n.216+17115A>G
XM_017017844.1:c.-440+17115A>G	XP_016873333.1:n.-440+17115A>G
NM_016931.5:c.153+17115A>G MANE Select	NP_058627.2:n.153+17115A>G
NM_001143836.3:c.153+17115A>G	NP_001137308.2:n.153+17115A>G
NM_001143837.2:c.81+17115A>G	NP_001137309.2:n.81+17115A>G
NM_001291926.2:c.-66+17115A>G	NP_001278855.2:n.-66+17115A>G
NM_001291929.2:c.78+17264A>G	NP_001278858.2:n.78+17264A>G