Canonical Allele Identifier: CA358573249

Gene: ETFDH

Linked Data

• MyVariant Identifiers: chr4:g.159601621T>C (hg19) ; chr4:g.158680469T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158680469T>C , CM000666.2:g.158680469T>C	GRCh38
NC_000004.11:g.159601621T>C , CM000666.1:g.159601621T>C	GRCh37
NC_000004.10:g.159821071T>C	NCBI36
NG_007078.2:g.13128T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436096.3:n.288T>C
ENST00000507475.6:n.179-4123T>C
ENST00000681978.1:n.286T>C
ENST00000682178.1:n.62T>C
ENST00000682345.1:c.35-59T>C	ENSP00000508122.1:n.35-59T>C
ENST00000682409.1:n.146T>C
ENST00000682452.1:n.368T>C
ENST00000682456.1:c.37T>C	ENSP00000508240.1:p.Tyr13His
ENST00000682601.1:n.228T>C
ENST00000682734.1:c.-649-4123T>C	ENSP00000507860.1:n.-649-4123T>C
ENST00000682820.1:n.74T>C
ENST00000682910.1:n.344T>C
ENST00000683004.1:c.37T>C	ENSP00000506936.1:p.Tyr13His
ENST00000683079.1:c.37T>C	ENSP00000507296.1:p.Tyr13His
ENST00000683081.1:c.37T>C	ENSP00000507722.1:p.Tyr13His
ENST00000683305.1:c.-52-1102T>C	ENSP00000508043.1:n.-52-1102T>C
ENST00000683448.1:c.-90-4123T>C	ENSP00000506931.1:n.-90-4123T>C
ENST00000683478.1:c.37T>C	ENSP00000507793.1:p.Tyr13His
ENST00000683483.1:c.37T>C	ENSP00000507719.1:p.Tyr13His
ENST00000683750.1:n.160T>C
ENST00000683751.1:c.-90-4123T>C	ENSP00000506944.1:n.-90-4123T>C
ENST00000683799.1:n.346T>C
ENST00000684036.1:c.-147T>C	ENSP00000507276.1:n.-147T>C
ENST00000684129.1:c.-694-4123T>C	ENSP00000507174.1:n.-694-4123T>C
ENST00000684209.1:n.277T>C
ENST00000684296.1:c.37T>C	ENSP00000507740.1:p.Tyr13His
ENST00000684505.1:c.37T>C	ENSP00000508237.1:p.Tyr13His
ENST00000684552.1:c.37T>C	ENSP00000506899.1:p.Tyr13His
ENST00000684611.1:n.178T>C
ENST00000684622.1:c.37T>C	ENSP00000507546.1:p.Tyr13His
ENST00000684627.1:c.-147T>C	ENSP00000507471.1:n.-147T>C
ENST00000684641.1:c.37T>C	ENSP00000507642.1:p.Tyr13His
ENST00000684675.1:c.37T>C	ENSP00000506934.1:p.Tyr13His
ENST00000684749.1:n.62T>C
ENST00000511912.6:c.37T>C MANE Select	ENSP00000426638.1:p.Tyr13His
ENST00000307738.5:c.35-1726T>C	ENSP00000303552.5:n.35-1726T>C
ENST00000436096.2:n.178T>C
ENST00000506422.1:n.86+7979T>C
ENST00000507475.5:c.-90-4123T>C	ENSP00000422735.1:n.-90-4123T>C
ENST00000511912.5:c.37T>C	ENSP00000426638.1:p.Tyr13His
ENST00000512251.5:c.35-59T>C	ENSP00000425661.1:n.35-59T>C
NM_001281737.1:c.35-1726T>C	NP_001268666.1:n.35-1726T>C
NM_004453.3:c.37T>C	NP_004444.2:p.Tyr13His
XM_024453935.1:c.-147T>C	XP_024309703.1:n.-147T>C
NM_004453.4:c.37T>C MANE Select	NP_004444.2:p.Tyr13His
NM_001281737.2:c.35-1726T>C	NP_001268666.1:n.35-1726T>C