Canonical Allele Identifier: CA812058960

Gene: NDUFS4

Linked Data

• dbSNP Id: rs777870422
• MyVariant Identifiers: chr5:g.52954347T>G (hg19) ; chr5:g.53658517T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658517T>G , CM000667.2:g.53658517T>G	GRCh38
NC_000005.9:g.52954347T>G , CM000667.1:g.52954347T>G	GRCh37
NC_000005.8:g.52990104T>G	NCBI36
NG_008200.1:g.102883T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.351-34T>G MANE Select	ENSP00000296684.5:n.351-34T>G
ENST00000296684.9:c.351-34T>G	ENSP00000296684.5:n.351-34T>G
ENST00000502423.5:c.*218-34T>G	ENSP00000422177.1:n.*218-34T>G
ENST00000506765.1:c.338+12112T>G	ENSP00000424570.1:n.338+12112T>G
ENST00000506974.5:c.*127-34T>G	ENSP00000425967.1:n.*127-34T>G
ENST00000507026.5:c.*325-34T>G	ENSP00000424993.1:n.*325-34T>G
ENST00000509443.1:n.212-34T>G
NM_002495.2:c.351-34T>G	NP_002486.1:n.351-34T>G
XM_005248525.3:c.350+12112T>G	XP_005248582.1:n.350+12112T>G
XM_011543415.1:c.177-34T>G	XP_011541717.1:n.177-34T>G
NM_001318051.1:c.350+12112T>G	NP_001304980.1:n.350+12112T>G
NM_002495.3:c.351-34T>G	NP_002486.1:n.351-34T>G
NR_134473.1:n.553-34T>G
NR_134474.1:n.470-34T>G
NR_134475.1:n.505-34T>G
NM_002495.4:c.351-34T>G MANE Select	NP_002486.1:n.351-34T>G
NM_001318051.2:c.350+12112T>G	NP_001304980.1:n.350+12112T>G
NR_134473.2:n.547-34T>G
NR_134474.2:n.464-34T>G
NR_134475.2:n.499-34T>G