Canonical Allele Identifier: CA359719039

Gene: NDUFS4

Linked Data

• gnomAD v4: 5-53560724-C-T
• MyVariant Identifiers: chr5:g.52856554C>T (hg19) ; chr5:g.53560724C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53560724C>T , CM000667.2:g.53560724C>T	GRCh38
NC_000005.9:g.52856554C>T , CM000667.1:g.52856554C>T	GRCh37
NC_000005.8:g.52892311C>T	NCBI36
NG_008200.1:g.5090C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.62C>T MANE Select	ENSP00000296684.5:p.Ala21Val
ENST00000296684.9:c.62C>T	ENSP00000296684.5:p.Ala21Val
ENST00000502423.5:c.62C>T	ENSP00000422177.1:p.Ala21Val
ENST00000506765.1:c.50C>T	ENSP00000424570.1:p.Ala17Val
ENST00000506974.5:c.62C>T	ENSP00000425967.1:p.Ala21Val
ENST00000507026.5:c.62C>T	ENSP00000424993.1:p.Ala21Val
NM_002495.2:c.62C>T	NP_002486.1:p.Ala21Val
XM_005248525.3:c.62C>T	XP_005248582.1:p.Ala21Val
XM_011543414.1:c.62C>T	XP_011541716.1:p.Ala21Val
NM_001318051.1:c.62C>T	NP_001304980.1:p.Ala21Val
NM_002495.3:c.62C>T	NP_002486.1:p.Ala21Val
NR_134473.1:n.92C>T
NR_134474.1:n.92C>T
NR_134475.1:n.92C>T
XM_017009491.1:c.62C>T	XP_016864980.1:p.Ala21Val
NM_002495.4:c.62C>T MANE Select	NP_002486.1:p.Ala21Val
NM_001318051.2:c.62C>T	NP_001304980.1:p.Ala21Val
NR_134473.2:n.86C>T
NR_134474.2:n.86C>T
NR_134475.2:n.86C>T