Canonical Allele Identifier: CA1546660792

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646205_53646207delinsCGT , CM000667.2:g.53646205_53646207delinsCGT	GRCh38
NC_000005.9:g.52942035_52942037delinsCGT , CM000667.1:g.52942035_52942037delinsCGT	GRCh37
NC_000005.8:g.52977792_52977794delinsCGT	NCBI36
NG_008200.1:g.90571_90573delinsCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.178-28_178-26delinsCGT MANE Select	ENSP00000296684.5:n.178-28_178-26delinsCGT
ENST00000296684.9:c.178-28_178-26delinsCGT	ENSP00000296684.5:n.178-28_178-26delinsCGT
ENST00000502423.5:c.*45-28_*45-26delinsCGT	ENSP00000422177.1:n.*45-28_*45-26delinsCGT
ENST00000506765.1:c.166-28_166-26delinsCGT	ENSP00000424570.1:n.166-28_166-26delinsCGT
ENST00000506974.5:c.350-28_350-26delinsCGT	ENSP00000425967.1:n.350-28_350-26delinsCGT
ENST00000507026.5:c.*152-28_*152-26delinsCGT	ENSP00000424993.1:n.*152-28_*152-26delinsCGT
ENST00000509443.1:n.11_13delinsCGT
NM_002495.2:c.178-28_178-26delinsCGT	NP_002486.1:n.178-28_178-26delinsCGT
XM_005248525.3:c.178-28_178-26delinsCGT	XP_005248582.1:n.178-28_178-26delinsCGT
XM_011543415.1:c.4-28_4-26delinsCGT	XP_011541717.1:n.4-28_4-26delinsCGT
NM_001318051.1:c.178-28_178-26delinsCGT	NP_001304980.1:n.178-28_178-26delinsCGT
NM_002495.3:c.178-28_178-26delinsCGT	NP_002486.1:n.178-28_178-26delinsCGT
NR_134473.1:n.380-28_380-26delinsCGT
NR_134474.1:n.297-28_297-26delinsCGT
NR_134475.1:n.332-28_332-26delinsCGT
NM_002495.4:c.178-28_178-26delinsCGT MANE Select	NP_002486.1:n.178-28_178-26delinsCGT
NM_001318051.2:c.178-28_178-26delinsCGT	NP_001304980.1:n.178-28_178-26delinsCGT
NR_134473.2:n.374-28_374-26delinsCGT
NR_134474.2:n.291-28_291-26delinsCGT
NR_134475.2:n.326-28_326-26delinsCGT