Canonical Allele Identifier: CA359719154

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52954401T>C (hg19) ; chr5:g.53658571T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658571T>C , CM000667.2:g.53658571T>C	GRCh38
NC_000005.9:g.52954401T>C , CM000667.1:g.52954401T>C	GRCh37
NC_000005.8:g.52990158T>C	NCBI36
NG_008200.1:g.102937T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.371T>C MANE Select	ENSP00000296684.5:p.Met124Thr
ENST00000296684.9:c.371T>C	ENSP00000296684.5:p.Met124Thr
ENST00000502423.5:c.*238T>C	ENSP00000422177.1:n.*238T>C
ENST00000506765.1:c.338+12166T>C	ENSP00000424570.1:n.338+12166T>C
ENST00000506974.5:c.*147T>C	ENSP00000425967.1:n.*147T>C
ENST00000507026.5:c.*345T>C	ENSP00000424993.1:n.*345T>C
ENST00000509443.1:n.232T>C
NM_002495.2:c.371T>C	NP_002486.1:p.Met124Thr
XM_005248525.3:c.350+12166T>C	XP_005248582.1:n.350+12166T>C
XM_011543415.1:c.197T>C	XP_011541717.1:p.Met66Thr
NM_001318051.1:c.350+12166T>C	NP_001304980.1:n.350+12166T>C
NM_002495.3:c.371T>C	NP_002486.1:p.Met124Thr
NR_134473.1:n.573T>C
NR_134474.1:n.490T>C
NR_134475.1:n.525T>C
NM_002495.4:c.371T>C MANE Select	NP_002486.1:p.Met124Thr
NM_001318051.2:c.350+12166T>C	NP_001304980.1:n.350+12166T>C
NR_134473.2:n.567T>C
NR_134474.2:n.484T>C
NR_134475.2:n.519T>C