Canonical Allele Identifier: CA1546620663

Gene: NDUFS4

Linked Data

• dbSNP Id: rs1748797318

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53560646del , CM000667.2:g.53560646del	GRCh38
NC_000005.9:g.52856476del , CM000667.1:g.52856476del	GRCh37
NC_000005.8:g.52892233del	NCBI36
NG_008200.1:g.5012del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.-17del MANE Select	ENSP00000296684.5:n.-17del
ENST00000296684.9:c.-17del	ENSP00000296684.5:n.-17del
ENST00000502423.5:c.-17del	ENSP00000422177.1:n.-17del
ENST00000507026.5:c.-17del	ENSP00000424993.1:n.-17del
NM_002495.2:c.-17del	NP_002486.1:n.-17del
XM_005248525.3:c.-17del	XP_005248582.1:n.-17del
XM_011543414.1:c.-17del	XP_011541716.1:n.-17del
NM_001318051.1:c.-17del	NP_001304980.1:n.-17del
NM_002495.3:c.-17del	NP_002486.1:n.-17del
NR_134473.1:n.14del
NR_134474.1:n.14del
NR_134475.1:n.14del
XM_017009491.1:c.-17del	XP_016864980.1:n.-17del
NM_002495.4:c.-17del MANE Select	NP_002486.1:n.-17del
NM_001318051.2:c.-17del	NP_001304980.1:n.-17del
NR_134473.2:n.8del
NR_134474.2:n.8del
NR_134475.2:n.8del