Canonical Allele Identifier: CA359719141

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52954395C>G (hg19) ; chr5:g.53658565C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658565C>G , CM000667.2:g.53658565C>G	GRCh38
NC_000005.9:g.52954395C>G , CM000667.1:g.52954395C>G	GRCh37
NC_000005.8:g.52990152C>G	NCBI36
NG_008200.1:g.102931C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.365C>G MANE Select	ENSP00000296684.5:p.Ser122Cys
ENST00000296684.9:c.365C>G	ENSP00000296684.5:p.Ser122Cys
ENST00000502423.5:c.*232C>G	ENSP00000422177.1:n.*232C>G
ENST00000506765.1:c.338+12160C>G	ENSP00000424570.1:n.338+12160C>G
ENST00000506974.5:c.*141C>G	ENSP00000425967.1:n.*141C>G
ENST00000507026.5:c.*339C>G	ENSP00000424993.1:n.*339C>G
ENST00000509443.1:n.226C>G
NM_002495.2:c.365C>G	NP_002486.1:p.Ser122Cys
XM_005248525.3:c.350+12160C>G	XP_005248582.1:n.350+12160C>G
XM_011543415.1:c.191C>G	XP_011541717.1:p.Ser64Cys
NM_001318051.1:c.350+12160C>G	NP_001304980.1:n.350+12160C>G
NM_002495.3:c.365C>G	NP_002486.1:p.Ser122Cys
NR_134473.1:n.567C>G
NR_134474.1:n.484C>G
NR_134475.1:n.519C>G
NM_002495.4:c.365C>G MANE Select	NP_002486.1:p.Ser122Cys
NM_001318051.2:c.350+12160C>G	NP_001304980.1:n.350+12160C>G
NR_134473.2:n.561C>G
NR_134474.2:n.478C>G
NR_134475.2:n.513C>G