Canonical Allele Identifier: CA1546620710

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53560700_53560703delinsCGTT , CM000667.2:g.53560700_53560703delinsCGTT	GRCh38
NC_000005.9:g.52856530_52856533delinsCGTT , CM000667.1:g.52856530_52856533delinsCGTT	GRCh37
NC_000005.8:g.52892287_52892290delinsCGTT	NCBI36
NG_008200.1:g.5066_5069delinsCGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.38_41delinsCGTT MANE Select	ENSP00000296684.5:p.Thr13=
ENST00000296684.9:c.38_41delinsCGTT	ENSP00000296684.5:p.Thr13=
ENST00000502423.5:c.38_41delinsCGTT	ENSP00000422177.1:p.Thr13=
ENST00000506765.1:c.26_29delinsCGTT	ENSP00000424570.1:p.Thr9=
ENST00000506974.5:c.38_41delinsCGTT	ENSP00000425967.1:p.Thr13=
ENST00000507026.5:c.38_41delinsCGTT	ENSP00000424993.1:p.Thr13=
NM_002495.2:c.38_41delinsCGTT	NP_002486.1:p.Thr13=
XM_005248525.3:c.38_41delinsCGTT	XP_005248582.1:p.Thr13=
XM_011543414.1:c.38_41delinsCGTT	XP_011541716.1:p.Thr13=
NM_001318051.1:c.38_41delinsCGTT	NP_001304980.1:p.Thr13=
NM_002495.3:c.38_41delinsCGTT	NP_002486.1:p.Thr13=
NR_134473.1:n.68_71delinsCGTT
NR_134474.1:n.68_71delinsCGTT
NR_134475.1:n.68_71delinsCGTT
XM_017009491.1:c.38_41delinsCGTT	XP_016864980.1:p.Thr13=
NM_002495.4:c.38_41delinsCGTT MANE Select	NP_002486.1:p.Thr13=
NM_001318051.2:c.38_41delinsCGTT	NP_001304980.1:p.Thr13=
NR_134473.2:n.62_65delinsCGTT
NR_134474.2:n.62_65delinsCGTT
NR_134475.2:n.62_65delinsCGTT