Canonical Allele Identifier: CA359719130

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52954391T>A (hg19) ; chr5:g.53658561T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658561T>A , CM000667.2:g.53658561T>A	GRCh38
NC_000005.9:g.52954391T>A , CM000667.1:g.52954391T>A	GRCh37
NC_000005.8:g.52990148T>A	NCBI36
NG_008200.1:g.102927T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.361T>A MANE Select	ENSP00000296684.5:p.Leu121Ile
ENST00000296684.9:c.361T>A	ENSP00000296684.5:p.Leu121Ile
ENST00000502423.5:c.*228T>A	ENSP00000422177.1:n.*228T>A
ENST00000506765.1:c.338+12156T>A	ENSP00000424570.1:n.338+12156T>A
ENST00000506974.5:c.*137T>A	ENSP00000425967.1:n.*137T>A
ENST00000507026.5:c.*335T>A	ENSP00000424993.1:n.*335T>A
ENST00000509443.1:n.222T>A
NM_002495.2:c.361T>A	NP_002486.1:p.Leu121Ile
XM_005248525.3:c.350+12156T>A	XP_005248582.1:n.350+12156T>A
XM_011543415.1:c.187T>A	XP_011541717.1:p.Leu63Ile
NM_001318051.1:c.350+12156T>A	NP_001304980.1:n.350+12156T>A
NM_002495.3:c.361T>A	NP_002486.1:p.Leu121Ile
NR_134473.1:n.563T>A
NR_134474.1:n.480T>A
NR_134475.1:n.515T>A
NM_002495.4:c.361T>A MANE Select	NP_002486.1:p.Leu121Ile
NM_001318051.2:c.350+12156T>A	NP_001304980.1:n.350+12156T>A
NR_134473.2:n.557T>A
NR_134474.2:n.474T>A
NR_134475.2:n.509T>A