Canonical Allele Identifier: CA358562754

Gene: ETFDH

Linked Data

• MyVariant Identifiers: chr4:g.159624599G>T (hg19) ; chr4:g.158703447G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158703447G>T , CM000666.2:g.158703447G>T	GRCh38
NC_000004.11:g.159624599G>T , CM000666.1:g.159624599G>T	GRCh37
NC_000004.10:g.159844049G>T	NCBI36
NG_007078.2:g.36106G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000681978.1:n.2677G>T
ENST00000682178.1:n.2173G>T
ENST00000682345.1:c.*841G>T	ENSP00000508122.1:n.*841G>T
ENST00000682452.1:n.1472G>T
ENST00000682456.1:c.1000G>T	ENSP00000508240.1:p.Gly334Cys
ENST00000682566.1:n.1924G>T
ENST00000682613.1:n.1453G>T
ENST00000682734.1:c.-33G>T	ENSP00000507860.1:n.-33G>T
ENST00000682820.1:n.1178G>T
ENST00000683004.1:c.*834G>T	ENSP00000506936.1:n.*834G>T
ENST00000683079.1:c.*566G>T	ENSP00000507296.1:n.*566G>T
ENST00000683081.1:c.*978G>T	ENSP00000507722.1:n.*978G>T
ENST00000683181.1:n.420G>T
ENST00000683209.1:n.3467G>T
ENST00000683305.1:c.958G>T	ENSP00000508043.1:p.Gly320Cys
ENST00000683448.1:c.*61G>T	ENSP00000506931.1:n.*61G>T
ENST00000683478.1:c.*492G>T	ENSP00000507793.1:n.*492G>T
ENST00000683483.1:c.997G>T	ENSP00000507719.1:p.Gly333Cys
ENST00000683622.1:n.855G>T
ENST00000683751.1:c.646G>T	ENSP00000506944.1:p.Gly216Cys
ENST00000684036.1:c.958G>T	ENSP00000507276.1:p.Gly320Cys
ENST00000684129.1:c.-33G>T	ENSP00000507174.1:n.-33G>T
ENST00000684209.1:n.1516G>T
ENST00000684296.1:c.*61G>T	ENSP00000507740.1:n.*61G>T
ENST00000684505.1:c.1090G>T	ENSP00000508237.1:p.Gly364Cys
ENST00000684552.1:c.*61G>T	ENSP00000506899.1:n.*61G>T
ENST00000684611.1:n.2869G>T
ENST00000684622.1:c.1141G>T	ENSP00000507546.1:p.Gly381Cys
ENST00000684627.1:c.958G>T	ENSP00000507471.1:p.Gly320Cys
ENST00000684641.1:c.856G>T	ENSP00000507642.1:p.Gly286Cys
ENST00000684675.1:c.1182G>T	ENSP00000506934.1:p.Leu394=
ENST00000684749.1:n.1210G>T
ENST00000511912.6:c.1141G>T MANE Select	ENSP00000426638.1:p.Gly381Cys
ENST00000307738.5:c.1000G>T	ENSP00000303552.5:p.Gly334Cys
ENST00000506422.1:n.111G>T
ENST00000511912.5:c.1141G>T	ENSP00000426638.1:p.Gly381Cys
NM_001281737.1:c.1000G>T	NP_001268666.1:p.Gly334Cys
NM_001281738.1:c.958G>T	NP_001268667.1:p.Gly320Cys
NM_004453.3:c.1141G>T	NP_004444.2:p.Gly381Cys
XM_024453935.1:c.958G>T	XP_024309703.1:p.Gly320Cys
NM_004453.4:c.1141G>T MANE Select	NP_004444.2:p.Gly381Cys
NM_001281737.2:c.1000G>T	NP_001268666.1:p.Gly334Cys