Canonical Allele Identifier: CA1546660816

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646242A= , CM000667.2:g.53646242A=	GRCh38
NC_000005.9:g.52942072A= , CM000667.1:g.52942072A=	GRCh37
NC_000005.8:g.52977829A=	NCBI36
NG_008200.1:g.90608A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.187A= MANE Select	ENSP00000296684.5:p.Thr63=
ENST00000296684.9:c.187A=	ENSP00000296684.5:p.Thr63=
ENST00000502423.5:c.*54A=	ENSP00000422177.1:n.*54A=
ENST00000506765.1:c.175A=	ENSP00000424570.1:p.Thr59=
ENST00000506974.5:c.359A=	ENSP00000425967.1:p.Tyr120=
ENST00000507026.5:c.*161A=	ENSP00000424993.1:n.*161A=
ENST00000509443.1:n.48A=
NM_002495.2:c.187A=	NP_002486.1:p.Thr63=
XM_005248525.3:c.187A=	XP_005248582.1:p.Thr63=
XM_011543415.1:c.13A=	XP_011541717.1:p.Thr5=
NM_001318051.1:c.187A=	NP_001304980.1:p.Thr63=
NM_002495.3:c.187A=	NP_002486.1:p.Thr63=
NR_134473.1:n.389A=
NR_134474.1:n.306A=
NR_134475.1:n.341A=
NM_002495.4:c.187A= MANE Select	NP_002486.1:p.Thr63=
NM_001318051.2:c.187A=	NP_001304980.1:p.Thr63=
NR_134473.2:n.383A=
NR_134474.2:n.300A=
NR_134475.2:n.335A=