Canonical Allele Identifier: CA359719062

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52856571G>T (hg19) ; chr5:g.53560741G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53560741G>T , CM000667.2:g.53560741G>T	GRCh38
NC_000005.9:g.52856571G>T , CM000667.1:g.52856571G>T	GRCh37
NC_000005.8:g.52892328G>T	NCBI36
NG_008200.1:g.5107G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.79G>T MANE Select	ENSP00000296684.5:p.Val27Phe
ENST00000296684.9:c.79G>T	ENSP00000296684.5:p.Val27Phe
ENST00000502423.5:c.79G>T	ENSP00000422177.1:p.Val27Phe
ENST00000506765.1:c.67G>T	ENSP00000424570.1:p.Val23Phe
ENST00000506974.5:c.79G>T	ENSP00000425967.1:p.Val27Phe
ENST00000507026.5:c.79G>T	ENSP00000424993.1:p.Val27Phe
NM_002495.2:c.79G>T	NP_002486.1:p.Val27Phe
XM_005248525.3:c.79G>T	XP_005248582.1:p.Val27Phe
XM_011543414.1:c.79G>T	XP_011541716.1:p.Val27Phe
NM_001318051.1:c.79G>T	NP_001304980.1:p.Val27Phe
NM_002495.3:c.79G>T	NP_002486.1:p.Val27Phe
NR_134473.1:n.109G>T
NR_134474.1:n.109G>T
NR_134475.1:n.109G>T
XM_017009491.1:c.79G>T	XP_016864980.1:p.Val27Phe
NM_002495.4:c.79G>T MANE Select	NP_002486.1:p.Val27Phe
NM_001318051.2:c.79G>T	NP_001304980.1:p.Val27Phe
NR_134473.2:n.103G>T
NR_134474.2:n.103G>T
NR_134475.2:n.103G>T