Canonical Allele Identifier: CA359719562

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52942076T>G (hg19) ; chr5:g.53646246T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646246T>G , CM000667.2:g.53646246T>G	GRCh38
NC_000005.9:g.52942076T>G , CM000667.1:g.52942076T>G	GRCh37
NC_000005.8:g.52977833T>G	NCBI36
NG_008200.1:g.90612T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.191T>G MANE Select	ENSP00000296684.5:p.Leu64Ter
ENST00000296684.9:c.191T>G	ENSP00000296684.5:p.Leu64Ter
ENST00000502423.5:c.*58T>G	ENSP00000422177.1:n.*58T>G
ENST00000506765.1:c.179T>G	ENSP00000424570.1:p.Leu60Ter
ENST00000506974.5:c.363T>G	ENSP00000425967.1:p.Phe121Leu
ENST00000507026.5:c.*165T>G	ENSP00000424993.1:n.*165T>G
ENST00000509443.1:n.52T>G
NM_002495.2:c.191T>G	NP_002486.1:p.Leu64Ter
XM_005248525.3:c.191T>G	XP_005248582.1:p.Leu64Ter
XM_011543415.1:c.17T>G	XP_011541717.1:p.Leu6Ter
NM_001318051.1:c.191T>G	NP_001304980.1:p.Leu64Ter
NM_002495.3:c.191T>G	NP_002486.1:p.Leu64Ter
NR_134473.1:n.393T>G
NR_134474.1:n.310T>G
NR_134475.1:n.345T>G
NM_002495.4:c.191T>G MANE Select	NP_002486.1:p.Leu64Ter
NM_001318051.2:c.191T>G	NP_001304980.1:p.Leu64Ter
NR_134473.2:n.387T>G
NR_134474.2:n.304T>G
NR_134475.2:n.339T>G