Canonical Allele Identifier: CA1506870462

Gene: ETFDH

Linked Data

• dbSNP Id: rs1773818917

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158680364_158680365dup , CM000666.2:g.158680364_158680365dup	GRCh38
NC_000004.11:g.159601516_159601517dup , CM000666.1:g.159601516_159601517dup	GRCh37
NC_000004.10:g.159820966_159820967dup	NCBI36
NG_007078.2:g.13023_13024dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436096.3:n.286-103_286-102dup
ENST00000507475.6:n.179-4228_179-4227dup
ENST00000681978.1:n.181_182dup
ENST00000682178.1:n.60-103_60-102dup
ENST00000682345.1:c.35-164_35-163dup	ENSP00000508122.1:n.35-164_35-163dup
ENST00000682409.1:n.144-103_144-102dup
ENST00000682452.1:n.263_264dup
ENST00000682456.1:c.35-103_35-102dup	ENSP00000508240.1:n.35-103_35-102dup
ENST00000682601.1:n.226-103_226-102dup
ENST00000682734.1:c.-649-4228_-649-4227dup	ENSP00000507860.1:n.-649-4228_-649-4227dup
ENST00000682820.1:n.72-103_72-102dup
ENST00000682910.1:n.239_240dup
ENST00000683004.1:c.35-103_35-102dup	ENSP00000506936.1:n.35-103_35-102dup
ENST00000683079.1:c.35-103_35-102dup	ENSP00000507296.1:n.35-103_35-102dup
ENST00000683081.1:c.35-103_35-102dup	ENSP00000507722.1:n.35-103_35-102dup
ENST00000683305.1:c.-52-1207_-52-1206dup	ENSP00000508043.1:n.-52-1207_-52-1206dup
ENST00000683448.1:c.-90-4228_-90-4227dup	ENSP00000506931.1:n.-90-4228_-90-4227dup
ENST00000683478.1:c.35-103_35-102dup	ENSP00000507793.1:n.35-103_35-102dup
ENST00000683483.1:c.35-103_35-102dup	ENSP00000507719.1:n.35-103_35-102dup
ENST00000683750.1:n.158-103_158-102dup
ENST00000683751.1:c.-90-4228_-90-4227dup	ENSP00000506944.1:n.-90-4228_-90-4227dup
ENST00000683799.1:n.241_242dup
ENST00000684036.1:c.-149-103_-149-102dup	ENSP00000507276.1:n.-149-103_-149-102dup
ENST00000684129.1:c.-694-4228_-694-4227dup	ENSP00000507174.1:n.-694-4228_-694-4227dup
ENST00000684209.1:n.172_173dup
ENST00000684296.1:c.35-103_35-102dup	ENSP00000507740.1:n.35-103_35-102dup
ENST00000684505.1:c.35-103_35-102dup	ENSP00000508237.1:n.35-103_35-102dup
ENST00000684552.1:c.35-103_35-102dup	ENSP00000506899.1:n.35-103_35-102dup
ENST00000684611.1:n.176-103_176-102dup
ENST00000684622.1:c.35-103_35-102dup	ENSP00000507546.1:n.35-103_35-102dup
ENST00000684627.1:c.-149-103_-149-102dup	ENSP00000507471.1:n.-149-103_-149-102dup
ENST00000684641.1:c.35-103_35-102dup	ENSP00000507642.1:n.35-103_35-102dup
ENST00000684675.1:c.35-103_35-102dup	ENSP00000506934.1:n.35-103_35-102dup
ENST00000684749.1:n.60-103_60-102dup
ENST00000511912.6:c.35-103_35-102dup MANE Select	ENSP00000426638.1:n.35-103_35-102dup
ENST00000307738.5:c.35-1831_35-1830dup	ENSP00000303552.5:n.35-1831_35-1830dup
ENST00000436096.2:n.176-103_176-102dup
ENST00000506422.1:n.86+7874_86+7875dup
ENST00000507475.5:c.-90-4228_-90-4227dup	ENSP00000422735.1:n.-90-4228_-90-4227dup
ENST00000511912.5:c.35-103_35-102dup	ENSP00000426638.1:n.35-103_35-102dup
ENST00000512251.5:c.35-164_35-163dup	ENSP00000425661.1:n.35-164_35-163dup
NM_001281737.1:c.35-1831_35-1830dup	NP_001268666.1:n.35-1831_35-1830dup
NM_004453.3:c.35-103_35-102dup	NP_004444.2:n.35-103_35-102dup
XM_024453935.1:c.-149-103_-149-102dup	XP_024309703.1:n.-149-103_-149-102dup
NM_004453.4:c.35-103_35-102dup MANE Select	NP_004444.2:n.35-103_35-102dup
NM_001281737.2:c.35-1831_35-1830dup	NP_001268666.1:n.35-1831_35-1830dup