Canonical Allele Identifier: CA359719537

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52942064A>T (hg19) ; chr5:g.53646234A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646234A>T , CM000667.2:g.53646234A>T	GRCh38
NC_000005.9:g.52942064A>T , CM000667.1:g.52942064A>T	GRCh37
NC_000005.8:g.52977821A>T	NCBI36
NG_008200.1:g.90600A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.179A>T MANE Select	ENSP00000296684.5:p.Asp60Val
ENST00000296684.9:c.179A>T	ENSP00000296684.5:p.Asp60Val
ENST00000502423.5:c.*46A>T	ENSP00000422177.1:n.*46A>T
ENST00000506765.1:c.167A>T	ENSP00000424570.1:p.Asp56Val
ENST00000506974.5:c.351A>T	ENSP00000425967.1:p.Gly117=
ENST00000507026.5:c.*153A>T	ENSP00000424993.1:n.*153A>T
ENST00000509443.1:n.40A>T
NM_002495.2:c.179A>T	NP_002486.1:p.Asp60Val
XM_005248525.3:c.179A>T	XP_005248582.1:p.Asp60Val
XM_011543415.1:c.5A>T	XP_011541717.1:p.Asp2Val
NM_001318051.1:c.179A>T	NP_001304980.1:p.Asp60Val
NM_002495.3:c.179A>T	NP_002486.1:p.Asp60Val
NR_134473.1:n.381A>T
NR_134474.1:n.298A>T
NR_134475.1:n.333A>T
NM_002495.4:c.179A>T MANE Select	NP_002486.1:p.Asp60Val
NM_001318051.2:c.179A>T	NP_001304980.1:p.Asp60Val
NR_134473.2:n.375A>T
NR_134474.2:n.292A>T
NR_134475.2:n.327A>T