Canonical Allele Identifier: CA1546660797
Gene: NDUFS4 HGNC NCBI

Linked Data

dbSNP Id: rs543590358

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53646208G>A , CM000667.2:g.53646208G>A GRCh38
NC_000005.9:g.52942038G>A , CM000667.1:g.52942038G>A GRCh37
NC_000005.8:g.52977795G>A NCBI36
NG_008200.1:g.90574G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296684.10:c.178-25G>A MANE Select ENSP00000296684.5:n.178-25G>A
ENST00000296684.9:c.178-25G>A ENSP00000296684.5:n.178-25G>A
ENST00000502423.5:c.*45-25G>A ENSP00000422177.1:n.*45-25G>A
ENST00000506765.1:c.166-25G>A ENSP00000424570.1:n.166-25G>A
ENST00000506974.5:c.350-25G>A ENSP00000425967.1:n.350-25G>A
ENST00000507026.5:c.*152-25G>A ENSP00000424993.1:n.*152-25G>A
ENST00000509443.1:n.14G>A
NM_002495.2:c.178-25G>A NP_002486.1:n.178-25G>A
XM_005248525.3:c.178-25G>A XP_005248582.1:n.178-25G>A
XM_011543415.1:c.4-25G>A XP_011541717.1:n.4-25G>A
NM_001318051.1:c.178-25G>A NP_001304980.1:n.178-25G>A
NM_002495.3:c.178-25G>A NP_002486.1:n.178-25G>A
NR_134473.1:n.380-25G>A
NR_134474.1:n.297-25G>A
NR_134475.1:n.332-25G>A
NM_002495.4:c.178-25G>A MANE Select NP_002486.1:n.178-25G>A
NM_001318051.2:c.178-25G>A NP_001304980.1:n.178-25G>A
NR_134473.2:n.374-25G>A
NR_134474.2:n.291-25G>A
NR_134475.2:n.326-25G>A