Canonical Allele Identifier: CA1546660781

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646184G= , CM000667.2:g.53646184G=	GRCh38
NC_000005.9:g.52942014G= , CM000667.1:g.52942014G=	GRCh37
NC_000005.8:g.52977771G=	NCBI36
NG_008200.1:g.90550G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.178-49G= MANE Select	ENSP00000296684.5:n.178-49G=
ENST00000296684.9:c.178-49G=	ENSP00000296684.5:n.178-49G=
ENST00000502423.5:c.*45-49G=	ENSP00000422177.1:n.*45-49G=
ENST00000506765.1:c.166-49G=	ENSP00000424570.1:n.166-49G=
ENST00000506974.5:c.350-49G=	ENSP00000425967.1:n.350-49G=
ENST00000507026.5:c.*152-49G=	ENSP00000424993.1:n.*152-49G=
NM_002495.2:c.178-49G=	NP_002486.1:n.178-49G=
XM_005248525.3:c.178-49G=	XP_005248582.1:n.178-49G=
XM_011543415.1:c.4-49G=	XP_011541717.1:n.4-49G=
NM_001318051.1:c.178-49G=	NP_001304980.1:n.178-49G=
NM_002495.3:c.178-49G=	NP_002486.1:n.178-49G=
NR_134473.1:n.380-49G=
NR_134474.1:n.297-49G=
NR_134475.1:n.332-49G=
NM_002495.4:c.178-49G= MANE Select	NP_002486.1:n.178-49G=
NM_001318051.2:c.178-49G=	NP_001304980.1:n.178-49G=
NR_134473.2:n.374-49G=
NR_134474.2:n.291-49G=
NR_134475.2:n.326-49G=