Canonical Allele Identifier: CA359719043
Gene: NDUFS4 HGNC NCBI

Linked Data

gnomAD v4: 5-53560727-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53560727T>C , CM000667.2:g.53560727T>C GRCh38
NC_000005.9:g.52856557T>C , CM000667.1:g.52856557T>C GRCh37
NC_000005.8:g.52892314T>C NCBI36
NG_008200.1:g.5093T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296684.10:c.65T>C MANE Select ENSP00000296684.5:p.Val22Ala
ENST00000296684.9:c.65T>C ENSP00000296684.5:p.Val22Ala
ENST00000502423.5:c.65T>C ENSP00000422177.1:p.Val22Ala
ENST00000506765.1:c.53T>C ENSP00000424570.1:p.Val18Ala
ENST00000506974.5:c.65T>C ENSP00000425967.1:p.Val22Ala
ENST00000507026.5:c.65T>C ENSP00000424993.1:p.Val22Ala
NM_002495.2:c.65T>C NP_002486.1:p.Val22Ala
XM_005248525.3:c.65T>C XP_005248582.1:p.Val22Ala
XM_011543414.1:c.65T>C XP_011541716.1:p.Val22Ala
NM_001318051.1:c.65T>C NP_001304980.1:p.Val22Ala
NM_002495.3:c.65T>C NP_002486.1:p.Val22Ala
NR_134473.1:n.95T>C
NR_134474.1:n.95T>C
NR_134475.1:n.95T>C
XM_017009491.1:c.65T>C XP_016864980.1:p.Val22Ala
NM_002495.4:c.65T>C MANE Select NP_002486.1:p.Val22Ala
NM_001318051.2:c.65T>C NP_001304980.1:p.Val22Ala
NR_134473.2:n.89T>C
NR_134474.2:n.89T>C
NR_134475.2:n.89T>C