Canonical Allele Identifier: CA3264127
Gene: NDUFS4 HGNC NCBI

Linked Data

dbSNP Id: rs769292531
gnomAD v2: 5-52856512-C-T
gnomAD v3: 5-53560682-C-T
gnomAD v4: 5-53560682-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53560682C>T , CM000667.2:g.53560682C>T GRCh38
NC_000005.9:g.52856512C>T , CM000667.1:g.52856512C>T GRCh37
NC_000005.8:g.52892269C>T NCBI36
NG_008200.1:g.5048C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296684.10:c.20C>T MANE Select ENSP00000296684.5:p.Ser7Leu
ENST00000296684.9:c.20C>T ENSP00000296684.5:p.Ser7Leu
ENST00000502423.5:c.20C>T ENSP00000422177.1:p.Ser7Leu
ENST00000506765.1:c.8C>T ENSP00000424570.1:p.Ser3Leu
ENST00000506974.5:c.20C>T ENSP00000425967.1:p.Ser7Leu
ENST00000507026.5:c.20C>T ENSP00000424993.1:p.Ser7Leu
NM_002495.2:c.20C>T NP_002486.1:p.Ser7Leu
XM_005248525.3:c.20C>T XP_005248582.1:p.Ser7Leu
XM_011543414.1:c.20C>T XP_011541716.1:p.Ser7Leu
NM_001318051.1:c.20C>T NP_001304980.1:p.Ser7Leu
NM_002495.3:c.20C>T NP_002486.1:p.Ser7Leu
NR_134473.1:n.50C>T
NR_134474.1:n.50C>T
NR_134475.1:n.50C>T
XM_017009491.1:c.20C>T XP_016864980.1:p.Ser7Leu
NM_002495.4:c.20C>T MANE Select NP_002486.1:p.Ser7Leu
NM_001318051.2:c.20C>T NP_001304980.1:p.Ser7Leu
NR_134473.2:n.44C>T
NR_134474.2:n.44C>T
NR_134475.2:n.44C>T