Canonical Allele Identifier: CA442141592

Gene: ETFDH

Linked Data

• MyVariant Identifiers: chr4:g.159601620A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158680468A>T , CM000666.2:g.158680468A>T	GRCh38
NC_000004.11:g.159601620A>T , CM000666.1:g.159601620A>T	GRCh37
NC_000004.10:g.159821070A>T	NCBI36
NG_007078.2:g.13127A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436096.3:n.287A>T
ENST00000507475.6:n.179-4124A>T
ENST00000681978.1:n.285A>T
ENST00000682178.1:n.61A>T
ENST00000682345.1:c.35-60A>T	ENSP00000508122.1:n.35-60A>T
ENST00000682409.1:n.145A>T
ENST00000682452.1:n.367A>T
ENST00000682456.1:c.36A>T	ENSP00000508240.1:p.Ala12=
ENST00000682601.1:n.227A>T
ENST00000682734.1:c.-649-4124A>T	ENSP00000507860.1:n.-649-4124A>T
ENST00000682820.1:n.73A>T
ENST00000682910.1:n.343A>T
ENST00000683004.1:c.36A>T	ENSP00000506936.1:p.Ala12=
ENST00000683079.1:c.36A>T	ENSP00000507296.1:p.Ala12=
ENST00000683081.1:c.36A>T	ENSP00000507722.1:p.Ala12=
ENST00000683305.1:c.-52-1103A>T	ENSP00000508043.1:n.-52-1103A>T
ENST00000683448.1:c.-90-4124A>T	ENSP00000506931.1:n.-90-4124A>T
ENST00000683478.1:c.36A>T	ENSP00000507793.1:p.Ala12=
ENST00000683483.1:c.36A>T	ENSP00000507719.1:p.Ala12=
ENST00000683750.1:n.159A>T
ENST00000683751.1:c.-90-4124A>T	ENSP00000506944.1:n.-90-4124A>T
ENST00000683799.1:n.345A>T
ENST00000684036.1:c.-148A>T	ENSP00000507276.1:n.-148A>T
ENST00000684129.1:c.-694-4124A>T	ENSP00000507174.1:n.-694-4124A>T
ENST00000684209.1:n.276A>T
ENST00000684296.1:c.36A>T	ENSP00000507740.1:p.Ala12=
ENST00000684505.1:c.36A>T	ENSP00000508237.1:p.Ala12=
ENST00000684552.1:c.36A>T	ENSP00000506899.1:p.Ala12=
ENST00000684611.1:n.177A>T
ENST00000684622.1:c.36A>T	ENSP00000507546.1:p.Ala12=
ENST00000684627.1:c.-148A>T	ENSP00000507471.1:n.-148A>T
ENST00000684641.1:c.36A>T	ENSP00000507642.1:p.Ala12=
ENST00000684675.1:c.36A>T	ENSP00000506934.1:p.Ala12=
ENST00000684749.1:n.61A>T
ENST00000511912.6:c.36A>T MANE Select	ENSP00000426638.1:p.Ala12=
ENST00000307738.5:c.35-1727A>T	ENSP00000303552.5:n.35-1727A>T
ENST00000436096.2:n.177A>T
ENST00000506422.1:n.86+7978A>T
ENST00000507475.5:c.-90-4124A>T	ENSP00000422735.1:n.-90-4124A>T
ENST00000511912.5:c.36A>T	ENSP00000426638.1:p.Ala12=
ENST00000512251.5:c.35-60A>T	ENSP00000425661.1:n.35-60A>T
NM_001281737.1:c.35-1727A>T	NP_001268666.1:n.35-1727A>T
NM_004453.3:c.36A>T	NP_004444.2:p.Ala12=
XM_024453935.1:c.-148A>T	XP_024309703.1:n.-148A>T
NM_004453.4:c.36A>T MANE Select	NP_004444.2:p.Ala12=
NM_001281737.2:c.35-1727A>T	NP_001268666.1:n.35-1727A>T