Canonical Allele Identifier: CA2673829306

Gene: NDUFS4

Linked Data

• gnomAD v4: 5-53658430-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658434del , CM000667.2:g.53658434del	GRCh38
NC_000005.9:g.52954264del , CM000667.1:g.52954264del	GRCh37
NC_000005.8:g.52990021del	NCBI36
NG_008200.1:g.102800del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.351-117del MANE Select	ENSP00000296684.5:n.351-117del
ENST00000296684.9:c.351-117del	ENSP00000296684.5:n.351-117del
ENST00000502423.5:c.*218-117del	ENSP00000422177.1:n.*218-117del
ENST00000506765.1:c.338+12029del	ENSP00000424570.1:n.338+12029del
ENST00000506974.5:c.*127-117del	ENSP00000425967.1:n.*127-117del
ENST00000507026.5:c.*325-117del	ENSP00000424993.1:n.*325-117del
ENST00000509443.1:n.212-117del
NM_002495.2:c.351-117del	NP_002486.1:n.351-117del
XM_005248525.3:c.350+12029del	XP_005248582.1:n.350+12029del
XM_011543415.1:c.177-117del	XP_011541717.1:n.177-117del
NM_001318051.1:c.350+12029del	NP_001304980.1:n.350+12029del
NM_002495.3:c.351-117del	NP_002486.1:n.351-117del
NR_134473.1:n.553-117del
NR_134474.1:n.470-117del
NR_134475.1:n.505-117del
NM_002495.4:c.351-117del MANE Select	NP_002486.1:n.351-117del
NM_001318051.2:c.350+12029del	NP_001304980.1:n.350+12029del
NR_134473.2:n.547-117del
NR_134474.2:n.464-117del
NR_134475.2:n.499-117del