Canonical Allele Identifier: CA1546660820

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646254G= , CM000667.2:g.53646254G=	GRCh38
NC_000005.9:g.52942084G= , CM000667.1:g.52942084G=	GRCh37
NC_000005.8:g.52977841G=	NCBI36
NG_008200.1:g.90620G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.199G= MANE Select	ENSP00000296684.5:p.Val67=
ENST00000296684.9:c.199G=	ENSP00000296684.5:p.Val67=
ENST00000502423.5:c.*66G=	ENSP00000422177.1:n.*66G=
ENST00000506765.1:c.187G=	ENSP00000424570.1:p.Val63=
ENST00000506974.5:c.371G=	ENSP00000425967.1:p.Ser124=
ENST00000507026.5:c.*173G=	ENSP00000424993.1:n.*173G=
ENST00000509443.1:n.60G=
NM_002495.2:c.199G=	NP_002486.1:p.Val67=
XM_005248525.3:c.199G=	XP_005248582.1:p.Val67=
XM_011543415.1:c.25G=	XP_011541717.1:p.Val9=
NM_001318051.1:c.199G=	NP_001304980.1:p.Val67=
NM_002495.3:c.199G=	NP_002486.1:p.Val67=
NR_134473.1:n.401G=
NR_134474.1:n.318G=
NR_134475.1:n.353G=
NM_002495.4:c.199G= MANE Select	NP_002486.1:p.Val67=
NM_001318051.2:c.199G=	NP_001304980.1:p.Val67=
NR_134473.2:n.395G=
NR_134474.2:n.312G=
NR_134475.2:n.347G=