Canonical Allele Identifier: CA1546660876

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646383C= , CM000667.2:g.53646383C=	GRCh38
NC_000005.9:g.52942213C= , CM000667.1:g.52942213C=	GRCh37
NC_000005.8:g.52977970C=	NCBI36
NG_008200.1:g.90749C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000296684.10:c.328C= MANE Select	ENSP00000296684.5:p.Pro110=
ENST00000296684.9:c.328C=	ENSP00000296684.5:p.Pro110=
ENST00000502423.5:c.*195C=	ENSP00000422177.1:n.*195C=
ENST00000506765.1:c.316C=	ENSP00000424570.1:p.Pro106=
ENST00000506974.5:c.*104C=	ENSP00000425967.1:n.*104C=
ENST00000507026.5:c.*302C=	ENSP00000424993.1:n.*302C=
ENST00000509443.1:n.189C=
NM_002495.2:c.328C=	NP_002486.1:p.Pro110=
XM_005248525.3:c.328C=	XP_005248582.1:p.Pro110=
XM_011543415.1:c.154C=	XP_011541717.1:p.Pro52=
NM_001318051.1:c.328C=	NP_001304980.1:p.Pro110=
NM_002495.3:c.328C=	NP_002486.1:p.Pro110=
NR_134473.1:n.530C=
NR_134474.1:n.447C=
NR_134475.1:n.482C=
NM_002495.4:c.328C= MANE Select	NP_002486.1:p.Pro110=
NM_001318051.2:c.328C=	NP_001304980.1:p.Pro110=
NR_134473.2:n.524C=
NR_134474.2:n.441C=
NR_134475.2:n.476C=