Canonical Allele Identifier: CA119135625

Gene: NDUFS4

Linked Data

• dbSNP Id: rs568858035
• gnomAD v3: 5-53646169-C-A
• gnomAD v4: 5-53646169-C-A
• MyVariant Identifiers: chr5:g.52941999C>A (hg19) ; chr5:g.53646169C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646169C>A , CM000667.2:g.53646169C>A	GRCh38
NC_000005.9:g.52941999C>A , CM000667.1:g.52941999C>A	GRCh37
NC_000005.8:g.52977756C>A	NCBI36
NG_008200.1:g.90535C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.178-64C>A MANE Select	ENSP00000296684.5:n.178-64C>A
ENST00000296684.9:c.178-64C>A	ENSP00000296684.5:n.178-64C>A
ENST00000502423.5:c.*45-64C>A	ENSP00000422177.1:n.*45-64C>A
ENST00000506765.1:c.166-64C>A	ENSP00000424570.1:n.166-64C>A
ENST00000506974.5:c.350-64C>A	ENSP00000425967.1:n.350-64C>A
ENST00000507026.5:c.*152-64C>A	ENSP00000424993.1:n.*152-64C>A
NM_002495.2:c.178-64C>A	NP_002486.1:n.178-64C>A
XM_005248525.3:c.178-64C>A	XP_005248582.1:n.178-64C>A
XM_011543415.1:c.4-64C>A	XP_011541717.1:n.4-64C>A
NM_001318051.1:c.178-64C>A	NP_001304980.1:n.178-64C>A
NM_002495.3:c.178-64C>A	NP_002486.1:n.178-64C>A
NR_134473.1:n.380-64C>A
NR_134474.1:n.297-64C>A
NR_134475.1:n.332-64C>A
NM_002495.4:c.178-64C>A MANE Select	NP_002486.1:n.178-64C>A
NM_001318051.2:c.178-64C>A	NP_001304980.1:n.178-64C>A
NR_134473.2:n.374-64C>A
NR_134474.2:n.291-64C>A
NR_134475.2:n.326-64C>A