Canonical Allele Identifier: CA359719723

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52942151C>G (hg19) ; chr5:g.53646321C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646321C>G , CM000667.2:g.53646321C>G	GRCh38
NC_000005.9:g.52942151C>G , CM000667.1:g.52942151C>G	GRCh37
NC_000005.8:g.52977908C>G	NCBI36
NG_008200.1:g.90687C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.266C>G MANE Select	ENSP00000296684.5:p.Ser89Cys
ENST00000296684.9:c.266C>G	ENSP00000296684.5:p.Ser89Cys
ENST00000502423.5:c.*133C>G	ENSP00000422177.1:n.*133C>G
ENST00000506765.1:c.254C>G	ENSP00000424570.1:p.Ser85Cys
ENST00000506974.5:c.*42C>G	ENSP00000425967.1:n.*42C>G
ENST00000507026.5:c.*240C>G	ENSP00000424993.1:n.*240C>G
ENST00000509443.1:n.127C>G
NM_002495.2:c.266C>G	NP_002486.1:p.Ser89Cys
XM_005248525.3:c.266C>G	XP_005248582.1:p.Ser89Cys
XM_011543415.1:c.92C>G	XP_011541717.1:p.Ser31Cys
NM_001318051.1:c.266C>G	NP_001304980.1:p.Ser89Cys
NM_002495.3:c.266C>G	NP_002486.1:p.Ser89Cys
NR_134473.1:n.468C>G
NR_134474.1:n.385C>G
NR_134475.1:n.420C>G
NM_002495.4:c.266C>G MANE Select	NP_002486.1:p.Ser89Cys
NM_001318051.2:c.266C>G	NP_001304980.1:p.Ser89Cys
NR_134473.2:n.462C>G
NR_134474.2:n.379C>G
NR_134475.2:n.414C>G