Canonical Allele Identifier: CA359719618
Gene: NDUFS4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53646273A>T , CM000667.2:g.53646273A>T GRCh38
NC_000005.9:g.52942103A>T , CM000667.1:g.52942103A>T GRCh37
NC_000005.8:g.52977860A>T NCBI36
NG_008200.1:g.90639A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296684.10:c.218A>T MANE Select ENSP00000296684.5:p.Lys73Ile
ENST00000296684.9:c.218A>T ENSP00000296684.5:p.Lys73Ile
ENST00000502423.5:c.*85A>T ENSP00000422177.1:n.*85A>T
ENST00000506765.1:c.206A>T ENSP00000424570.1:p.Lys69Ile
ENST00000506974.5:c.390A>T ENSP00000425967.1:p.Lys130Asn
ENST00000507026.5:c.*192A>T ENSP00000424993.1:n.*192A>T
ENST00000509443.1:n.79A>T
NM_002495.2:c.218A>T NP_002486.1:p.Lys73Ile
XM_005248525.3:c.218A>T XP_005248582.1:p.Lys73Ile
XM_011543415.1:c.44A>T XP_011541717.1:p.Lys15Ile
NM_001318051.1:c.218A>T NP_001304980.1:p.Lys73Ile
NM_002495.3:c.218A>T NP_002486.1:p.Lys73Ile
NR_134473.1:n.420A>T
NR_134474.1:n.337A>T
NR_134475.1:n.372A>T
NM_002495.4:c.218A>T MANE Select NP_002486.1:p.Lys73Ile
NM_001318051.2:c.218A>T NP_001304980.1:p.Lys73Ile
NR_134473.2:n.414A>T
NR_134474.2:n.331A>T
NR_134475.2:n.366A>T