Canonical Allele Identifier: CA444330364

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52942152T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646322T>G , CM000667.2:g.53646322T>G	GRCh38
NC_000005.9:g.52942152T>G , CM000667.1:g.52942152T>G	GRCh37
NC_000005.8:g.52977909T>G	NCBI36
NG_008200.1:g.90688T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.267T>G MANE Select	ENSP00000296684.5:p.Ser89=
ENST00000296684.9:c.267T>G	ENSP00000296684.5:p.Ser89=
ENST00000502423.5:c.*134T>G	ENSP00000422177.1:n.*134T>G
ENST00000506765.1:c.255T>G	ENSP00000424570.1:p.Ser85=
ENST00000506974.5:c.*43T>G	ENSP00000425967.1:n.*43T>G
ENST00000507026.5:c.*241T>G	ENSP00000424993.1:n.*241T>G
ENST00000509443.1:n.128T>G
NM_002495.2:c.267T>G	NP_002486.1:p.Ser89=
XM_005248525.3:c.267T>G	XP_005248582.1:p.Ser89=
XM_011543415.1:c.93T>G	XP_011541717.1:p.Ser31=
NM_001318051.1:c.267T>G	NP_001304980.1:p.Ser89=
NM_002495.3:c.267T>G	NP_002486.1:p.Ser89=
NR_134473.1:n.469T>G
NR_134474.1:n.386T>G
NR_134475.1:n.421T>G
NM_002495.4:c.267T>G MANE Select	NP_002486.1:p.Ser89=
NM_001318051.2:c.267T>G	NP_001304980.1:p.Ser89=
NR_134473.2:n.463T>G
NR_134474.2:n.380T>G
NR_134475.2:n.415T>G