Canonical Allele Identifier: CA1546660875

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646382T= , CM000667.2:g.53646382T=	GRCh38
NC_000005.9:g.52942212T= , CM000667.1:g.52942212T=	GRCh37
NC_000005.8:g.52977969T=	NCBI36
NG_008200.1:g.90748T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000296684.10:c.327T= MANE Select	ENSP00000296684.5:p.Asn109=
ENST00000296684.9:c.327T=	ENSP00000296684.5:p.Asn109=
ENST00000502423.5:c.*194T=	ENSP00000422177.1:n.*194T=
ENST00000506765.1:c.315T=	ENSP00000424570.1:p.Asn105=
ENST00000506974.5:c.*103T=	ENSP00000425967.1:n.*103T=
ENST00000507026.5:c.*301T=	ENSP00000424993.1:n.*301T=
ENST00000509443.1:n.188T=
NM_002495.2:c.327T=	NP_002486.1:p.Asn109=
XM_005248525.3:c.327T=	XP_005248582.1:p.Asn109=
XM_011543415.1:c.153T=	XP_011541717.1:p.Asn51=
NM_001318051.1:c.327T=	NP_001304980.1:p.Asn109=
NM_002495.3:c.327T=	NP_002486.1:p.Asn109=
NR_134473.1:n.529T=
NR_134474.1:n.446T=
NR_134475.1:n.481T=
NM_002495.4:c.327T= MANE Select	NP_002486.1:p.Asn109=
NM_001318051.2:c.327T=	NP_001304980.1:p.Asn109=
NR_134473.2:n.523T=
NR_134474.2:n.440T=
NR_134475.2:n.475T=