Canonical Allele Identifier: CA1546660791
Gene: NDUFS4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53646202A= , CM000667.2:g.53646202A= GRCh38
NC_000005.9:g.52942032A= , CM000667.1:g.52942032A= GRCh37
NC_000005.8:g.52977789A= NCBI36
NG_008200.1:g.90568A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296684.10:c.178-31A= MANE Select ENSP00000296684.5:n.178-31A=
ENST00000296684.9:c.178-31A= ENSP00000296684.5:n.178-31A=
ENST00000502423.5:c.*45-31A= ENSP00000422177.1:n.*45-31A=
ENST00000506765.1:c.166-31A= ENSP00000424570.1:n.166-31A=
ENST00000506974.5:c.350-31A= ENSP00000425967.1:n.350-31A=
ENST00000507026.5:c.*152-31A= ENSP00000424993.1:n.*152-31A=
ENST00000509443.1:n.8A=
NM_002495.2:c.178-31A= NP_002486.1:n.178-31A=
XM_005248525.3:c.178-31A= XP_005248582.1:n.178-31A=
XM_011543415.1:c.4-31A= XP_011541717.1:n.4-31A=
NM_001318051.1:c.178-31A= NP_001304980.1:n.178-31A=
NM_002495.3:c.178-31A= NP_002486.1:n.178-31A=
NR_134473.1:n.380-31A=
NR_134474.1:n.297-31A=
NR_134475.1:n.332-31A=
NM_002495.4:c.178-31A= MANE Select NP_002486.1:n.178-31A=
NM_001318051.2:c.178-31A= NP_001304980.1:n.178-31A=
NR_134473.2:n.374-31A=
NR_134474.2:n.291-31A=
NR_134475.2:n.326-31A=