Canonical Allele Identifier: CA3122330

Gene: ETFDH

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158682408A>T , CM000666.2:g.158682408A>T	GRCh38
NC_000004.11:g.159603560A>T , CM000666.1:g.159603560A>T	GRCh37
NC_000004.10:g.159823010A>T	NCBI36
NG_007078.2:g.15067A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004453.4:c.389A>T MANE Select	NP_004444.2:p.Asp130Val
ENST00000511912.6:c.389A>T MANE Select	ENSP00000426638.1:p.Asp130Val
NM_001281737.1:c.248A>T	NP_001268666.1:p.Asp83Val
NM_001281737.2:c.248A>T	NP_001268666.1:p.Asp83Val
NM_001281738.1:c.206A>T	NP_001268667.1:p.Asp69Val
NM_004453.3:c.389A>T	NP_004444.2:p.Asp130Val
ENST00000307738.5:c.248A>T	ENSP00000303552.5:p.Asp83Val
ENST00000436096.2:n.574A>T
ENST00000436096.3:n.640A>T
ENST00000506422.1:n.86+9918A>T
ENST00000507475.5:c.-90-2184A>T	ENSP00000422735.1:n.-90-2184A>T
ENST00000507475.6:n.179-2184A>T
ENST00000511912.5:c.389A>T	ENSP00000426638.1:p.Asp130Val
ENST00000514148.1:n.467A>T
ENST00000681978.1:n.638A>T
ENST00000682178.1:n.1421A>T
ENST00000682345.1:c.*208A>T	ENSP00000508122.1:n.*208A>T
ENST00000682409.1:n.2085A>T
ENST00000682452.1:n.720A>T
ENST00000682456.1:c.389A>T	ENSP00000508240.1:p.Asp130Val
ENST00000682601.1:n.580A>T
ENST00000682734.1:c.-649-2184A>T	ENSP00000507860.1:n.-649-2184A>T
ENST00000682820.1:n.426A>T
ENST00000682910.1:n.696A>T
ENST00000683004.1:c.*226A>T	ENSP00000506936.1:n.*226A>T
ENST00000683079.1:c.389A>T	ENSP00000507296.1:p.Asp130Val
ENST00000683081.1:c.*226A>T	ENSP00000507722.1:n.*226A>T
ENST00000683123.1:n.11A>T
ENST00000683305.1:c.206A>T	ENSP00000508043.1:p.Asp69Val
ENST00000683448.1:c.-90-2184A>T	ENSP00000506931.1:n.-90-2184A>T
ENST00000683478.1:c.389A>T	ENSP00000507793.1:p.Asp130Val
ENST00000683483.1:c.389A>T	ENSP00000507719.1:p.Asp130Val
ENST00000683750.1:n.512A>T
ENST00000683751.1:c.-90-2184A>T	ENSP00000506944.1:n.-90-2184A>T
ENST00000683799.1:n.1705A>T
ENST00000684036.1:c.206A>T	ENSP00000507276.1:p.Asp69Val
ENST00000684129.1:c.-694-2184A>T	ENSP00000507174.1:n.-694-2184A>T
ENST00000684209.1:n.629A>T
ENST00000684296.1:c.389A>T	ENSP00000507740.1:p.Asp130Val
ENST00000684505.1:c.389A>T	ENSP00000508237.1:p.Asp130Val
ENST00000684552.1:c.389A>T	ENSP00000506899.1:p.Asp130Val
ENST00000684611.1:n.2117A>T
ENST00000684622.1:c.389A>T	ENSP00000507546.1:p.Asp130Val
ENST00000684627.1:c.206A>T	ENSP00000507471.1:p.Asp69Val
ENST00000684641.1:c.389A>T	ENSP00000507642.1:p.Asp130Val
ENST00000684675.1:c.389A>T	ENSP00000506934.1:p.Asp130Val
ENST00000684749.1:n.458A>T
XM_024453935.1:c.206A>T	XP_024309703.1:p.Asp69Val