Canonical Allele Identifier: CA1546666276

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658565C= , CM000667.2:g.53658565C=	GRCh38
NC_000005.9:g.52954395C= , CM000667.1:g.52954395C=	GRCh37
NC_000005.8:g.52990152C=	NCBI36
NG_008200.1:g.102931C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.365C= MANE Select	ENSP00000296684.5:p.Ser122=
ENST00000296684.9:c.365C=	ENSP00000296684.5:p.Ser122=
ENST00000502423.5:c.*232C=	ENSP00000422177.1:n.*232C=
ENST00000506765.1:c.338+12160C=	ENSP00000424570.1:n.338+12160C=
ENST00000506974.5:c.*141C=	ENSP00000425967.1:n.*141C=
ENST00000507026.5:c.*339C=	ENSP00000424993.1:n.*339C=
ENST00000509443.1:n.226C=
NM_002495.2:c.365C=	NP_002486.1:p.Ser122=
XM_005248525.3:c.350+12160C=	XP_005248582.1:n.350+12160C=
XM_011543415.1:c.191C=	XP_011541717.1:p.Ser64=
NM_001318051.1:c.350+12160C=	NP_001304980.1:n.350+12160C=
NM_002495.3:c.365C=	NP_002486.1:p.Ser122=
NR_134473.1:n.567C=
NR_134474.1:n.484C=
NR_134475.1:n.519C=
NM_002495.4:c.365C= MANE Select	NP_002486.1:p.Ser122=
NM_001318051.2:c.350+12160C=	NP_001304980.1:n.350+12160C=
NR_134473.2:n.561C=
NR_134474.2:n.478C=
NR_134475.2:n.513C=