Canonical Allele Identifier: CA812059475
Gene: NDUFS4 HGNC NCBI

Linked Data

dbSNP Id: rs1396317176
gnomAD v3: 5-53658825-C-G
gnomAD v4: 5-53658825-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53658825C>G , CM000667.2:g.53658825C>G GRCh38
NC_000005.9:g.52954655C>G , CM000667.1:g.52954655C>G GRCh37
NC_000005.8:g.52990412C>G NCBI36
NG_008200.1:g.103191C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296684.10:c.424+201C>G MANE Select ENSP00000296684.5:n.424+201C>G
ENST00000296684.9:c.424+201C>G ENSP00000296684.5:n.424+201C>G
ENST00000502423.5:c.*291+201C>G ENSP00000422177.1:n.*291+201C>G
ENST00000506765.1:c.338+12420C>G ENSP00000424570.1:n.338+12420C>G
ENST00000506974.5:c.*200+201C>G ENSP00000425967.1:n.*200+201C>G
ENST00000507026.5:c.*398+201C>G ENSP00000424993.1:n.*398+201C>G
NM_002495.2:c.424+201C>G NP_002486.1:n.424+201C>G
XM_005248525.3:c.350+12420C>G XP_005248582.1:n.350+12420C>G
XM_011543415.1:c.250+201C>G XP_011541717.1:n.250+201C>G
NM_001318051.1:c.350+12420C>G NP_001304980.1:n.350+12420C>G
NM_002495.3:c.424+201C>G NP_002486.1:n.424+201C>G
NR_134473.1:n.626+201C>G
NR_134474.1:n.543+201C>G
NR_134475.1:n.578+201C>G
NM_002495.4:c.424+201C>G MANE Select NP_002486.1:n.424+201C>G
NM_001318051.2:c.350+12420C>G NP_001304980.1:n.350+12420C>G
NR_134473.2:n.620+201C>G
NR_134474.2:n.537+201C>G
NR_134475.2:n.572+201C>G