Canonical Allele Identifier: CA359719062
Gene: NDUFS4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53560741G>T , CM000667.2:g.53560741G>T GRCh38
NC_000005.9:g.52856571G>T , CM000667.1:g.52856571G>T GRCh37
NC_000005.8:g.52892328G>T NCBI36
NG_008200.1:g.5107G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296684.10:c.79G>T MANE Select ENSP00000296684.5:p.Val27Phe
ENST00000296684.9:c.79G>T ENSP00000296684.5:p.Val27Phe
ENST00000502423.5:c.79G>T ENSP00000422177.1:p.Val27Phe
ENST00000506765.1:c.67G>T ENSP00000424570.1:p.Val23Phe
ENST00000506974.5:c.79G>T ENSP00000425967.1:p.Val27Phe
ENST00000507026.5:c.79G>T ENSP00000424993.1:p.Val27Phe
NM_002495.2:c.79G>T NP_002486.1:p.Val27Phe
XM_005248525.3:c.79G>T XP_005248582.1:p.Val27Phe
XM_011543414.1:c.79G>T XP_011541716.1:p.Val27Phe
NM_001318051.1:c.79G>T NP_001304980.1:p.Val27Phe
NM_002495.3:c.79G>T NP_002486.1:p.Val27Phe
NR_134473.1:n.109G>T
NR_134474.1:n.109G>T
NR_134475.1:n.109G>T
XM_017009491.1:c.79G>T XP_016864980.1:p.Val27Phe
NM_002495.4:c.79G>T MANE Select NP_002486.1:p.Val27Phe
NM_001318051.2:c.79G>T NP_001304980.1:p.Val27Phe
NR_134473.2:n.103G>T
NR_134474.2:n.103G>T
NR_134475.2:n.103G>T