Canonical Allele Identifier: CA3122455

Gene: ETFDH

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158695647T>C , CM000666.2:g.158695647T>C	GRCh38
NC_000004.11:g.159616799T>C , CM000666.1:g.159616799T>C	GRCh37
NC_000004.10:g.159836249T>C	NCBI36
NG_007078.2:g.28306T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004453.4:c.831+4T>C MANE Select	NP_004444.2:n.831+4T>C
ENST00000511912.6:c.831+4T>C MANE Select	ENSP00000426638.1:n.831+4T>C
NM_001281737.1:c.690+4T>C	NP_001268666.1:n.690+4T>C
NM_001281737.2:c.690+4T>C	NP_001268666.1:n.690+4T>C
NM_001281738.1:c.648+4T>C	NP_001268667.1:n.648+4T>C
NM_004453.3:c.831+4T>C	NP_004444.2:n.831+4T>C
ENST00000307738.5:c.690+4T>C	ENSP00000303552.5:n.690+4T>C
ENST00000506422.1:n.87-7776T>C
ENST00000507475.5:c.336+4T>C	ENSP00000422735.1:n.336+4T>C
ENST00000507475.6:n.604+4T>C
ENST00000511912.5:c.831+4T>C	ENSP00000426638.1:n.831+4T>C
ENST00000681978.1:n.1080+4T>C
ENST00000682178.1:n.1863+4T>C
ENST00000682345.1:c.*531+4T>C	ENSP00000508122.1:n.*531+4T>C
ENST00000682452.1:n.1162+4T>C
ENST00000682456.1:c.831+4T>C	ENSP00000508240.1:n.831+4T>C
ENST00000682566.1:n.327+4T>C
ENST00000682601.1:n.1022+4T>C
ENST00000682613.1:n.1143+4T>C
ENST00000682734.1:c.-343+4T>C	ENSP00000507860.1:n.-343+4T>C
ENST00000682820.1:n.868+4T>C
ENST00000683004.1:c.*668+4T>C	ENSP00000506936.1:n.*668+4T>C
ENST00000683079.1:c.*211+4T>C	ENSP00000507296.1:n.*211+4T>C
ENST00000683081.1:c.*668+4T>C	ENSP00000507722.1:n.*668+4T>C
ENST00000683305.1:c.648+4T>C	ENSP00000508043.1:n.648+4T>C
ENST00000683448.1:c.336+4T>C	ENSP00000506931.1:n.336+4T>C
ENST00000683478.1:c.*211+4T>C	ENSP00000507793.1:n.*211+4T>C
ENST00000683483.1:c.831+4T>C	ENSP00000507719.1:n.831+4T>C
ENST00000683751.1:c.336+4T>C	ENSP00000506944.1:n.336+4T>C
ENST00000684036.1:c.648+4T>C	ENSP00000507276.1:n.648+4T>C
ENST00000684129.1:c.-388+4T>C	ENSP00000507174.1:n.-388+4T>C
ENST00000684209.1:n.1206+4T>C
ENST00000684296.1:c.831+4T>C	ENSP00000507740.1:n.831+4T>C
ENST00000684505.1:c.780+4T>C	ENSP00000508237.1:n.780+4T>C
ENST00000684552.1:c.831+4T>C	ENSP00000506899.1:n.831+4T>C
ENST00000684611.1:n.2559+4T>C
ENST00000684622.1:c.831+4T>C	ENSP00000507546.1:n.831+4T>C
ENST00000684627.1:c.648+4T>C	ENSP00000507471.1:n.648+4T>C
ENST00000684641.1:c.831+4T>C	ENSP00000507642.1:n.831+4T>C
ENST00000684675.1:c.831+4T>C	ENSP00000506934.1:n.831+4T>C
ENST00000684749.1:n.900+4T>C
XM_024453935.1:c.648+4T>C	XP_024309703.1:n.648+4T>C