Canonical Allele Identifier: CA359719668

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52942125T>G (hg19) ; chr5:g.53646295T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646295T>G , CM000667.2:g.53646295T>G	GRCh38
NC_000005.9:g.52942125T>G , CM000667.1:g.52942125T>G	GRCh37
NC_000005.8:g.52977882T>G	NCBI36
NG_008200.1:g.90661T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.240T>G MANE Select	ENSP00000296684.5:p.Phe80Leu
ENST00000296684.9:c.240T>G	ENSP00000296684.5:p.Phe80Leu
ENST00000502423.5:c.*107T>G	ENSP00000422177.1:n.*107T>G
ENST00000506765.1:c.228T>G	ENSP00000424570.1:p.Phe76Leu
ENST00000506974.5:c.*16T>G	ENSP00000425967.1:n.*16T>G
ENST00000507026.5:c.*214T>G	ENSP00000424993.1:n.*214T>G
ENST00000509443.1:n.101T>G
NM_002495.2:c.240T>G	NP_002486.1:p.Phe80Leu
XM_005248525.3:c.240T>G	XP_005248582.1:p.Phe80Leu
XM_011543415.1:c.66T>G	XP_011541717.1:p.Phe22Leu
NM_001318051.1:c.240T>G	NP_001304980.1:p.Phe80Leu
NM_002495.3:c.240T>G	NP_002486.1:p.Phe80Leu
NR_134473.1:n.442T>G
NR_134474.1:n.359T>G
NR_134475.1:n.394T>G
NM_002495.4:c.240T>G MANE Select	NP_002486.1:p.Phe80Leu
NM_001318051.2:c.240T>G	NP_001304980.1:p.Phe80Leu
NR_134473.2:n.436T>G
NR_134474.2:n.353T>G
NR_134475.2:n.388T>G