Canonical Allele Identifier: CA2185263354

Gene: NOX5

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.69054606T>G , CM000677.2:g.69054606T>G	GRCh38
NC_000015.9:g.69346946T>G , CM000677.1:g.69346946T>G	GRCh37
NC_000015.8:g.67134000T>G	NCBI36
NG_030464.1:g.129108T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530406.7:c.1916-728T>G	ENSP00000432440.2:n.1916-728T>G
ENST00000703585.1:c.1895-728T>G	ENSP00000515387.1:n.1895-728T>G
ENST00000388866.8:c.2000-728T>G MANE Select	ENSP00000373518.3:n.2000-728T>G
ENST00000260364.9:c.1946-728T>G	ENSP00000454143.1:n.1946-728T>G
ENST00000388866.7:c.2000-728T>G	ENSP00000373518.3:n.2000-728T>G
ENST00000448182.7:c.1862-728T>G	ENSP00000410887.3:n.1862-728T>G
ENST00000455873.7:c.1895-728T>G	ENSP00000416828.3:n.1895-728T>G
ENST00000525143.5:c.1267-728T>G	ENSP00000455703.1:n.1267-728T>G
ENST00000527315.5:n.5156-728T>G
ENST00000529367.1:n.632-728T>G
ENST00000530406.6:c.1916-728T>G	ENSP00000432440.2:n.1916-728T>G
NM_001184779.1:c.1916-728T>G	NP_001171708.1:n.1916-728T>G
NM_001184780.1:c.1895-728T>G	NP_001171709.1:n.1895-728T>G
NM_024505.3:c.2000-728T>G	NP_078781.3:n.2000-728T>G
NR_033671.2:n.2272-728T>G
NR_033672.1:n.2188-728T>G
NM_024505.4:c.2000-728T>G MANE Select	NP_078781.3:n.2000-728T>G
NM_001184779.2:c.1916-728T>G	NP_001171708.1:n.1916-728T>G
NM_001184780.2:c.1895-728T>G	NP_001171709.1:n.1895-728T>G
NR_033671.3:n.2247-728T>G
NR_033672.2:n.2163-728T>G