Canonical Allele Identifier: CA2672515961

Gene: ETFDH

Linked Data

• gnomAD v4: 4-158703347-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158703347A>T , CM000666.2:g.158703347A>T	GRCh38
NC_000004.11:g.159624499A>T , CM000666.1:g.159624499A>T	GRCh37
NC_000004.10:g.159843949A>T	NCBI36
NG_007078.2:g.36006A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000681978.1:n.2653-76A>T
ENST00000682178.1:n.2149-76A>T
ENST00000682345.1:c.*817-76A>T	ENSP00000508122.1:n.*817-76A>T
ENST00000682452.1:n.1448-76A>T
ENST00000682456.1:c.976-76A>T	ENSP00000508240.1:n.976-76A>T
ENST00000682566.1:n.1900-76A>T
ENST00000682613.1:n.1429-76A>T
ENST00000682734.1:c.-57-76A>T	ENSP00000507860.1:n.-57-76A>T
ENST00000682820.1:n.1154-76A>T
ENST00000683004.1:c.*810-76A>T	ENSP00000506936.1:n.*810-76A>T
ENST00000683079.1:c.*542-76A>T	ENSP00000507296.1:n.*542-76A>T
ENST00000683081.1:c.*954-76A>T	ENSP00000507722.1:n.*954-76A>T
ENST00000683181.1:n.396-76A>T
ENST00000683209.1:n.3367A>T
ENST00000683305.1:c.934-76A>T	ENSP00000508043.1:n.934-76A>T
ENST00000683448.1:c.*37-76A>T	ENSP00000506931.1:n.*37-76A>T
ENST00000683478.1:c.*468-76A>T	ENSP00000507793.1:n.*468-76A>T
ENST00000683483.1:c.973-76A>T	ENSP00000507719.1:n.973-76A>T
ENST00000683622.1:n.755A>T
ENST00000683751.1:c.622-76A>T	ENSP00000506944.1:n.622-76A>T
ENST00000684036.1:c.934-76A>T	ENSP00000507276.1:n.934-76A>T
ENST00000684129.1:c.-57-76A>T	ENSP00000507174.1:n.-57-76A>T
ENST00000684209.1:n.1492-76A>T
ENST00000684296.1:c.*37-76A>T	ENSP00000507740.1:n.*37-76A>T
ENST00000684505.1:c.1066-76A>T	ENSP00000508237.1:n.1066-76A>T
ENST00000684552.1:c.*37-76A>T	ENSP00000506899.1:n.*37-76A>T
ENST00000684611.1:n.2845-76A>T
ENST00000684622.1:c.1117-76A>T	ENSP00000507546.1:n.1117-76A>T
ENST00000684627.1:c.934-76A>T	ENSP00000507471.1:n.934-76A>T
ENST00000684641.1:c.832-76A>T	ENSP00000507642.1:n.832-76A>T
ENST00000684675.1:c.1158-76A>T	ENSP00000506934.1:n.1158-76A>T
ENST00000684749.1:n.1186-76A>T
ENST00000511912.6:c.1117-76A>T MANE Select	ENSP00000426638.1:n.1117-76A>T
ENST00000307738.5:c.976-76A>T	ENSP00000303552.5:n.976-76A>T
ENST00000506422.1:n.87-76A>T
ENST00000511912.5:c.1117-76A>T	ENSP00000426638.1:n.1117-76A>T
NM_001281737.1:c.976-76A>T	NP_001268666.1:n.976-76A>T
NM_001281738.1:c.934-76A>T	NP_001268667.1:n.934-76A>T
NM_004453.3:c.1117-76A>T	NP_004444.2:n.1117-76A>T
XM_024453935.1:c.934-76A>T	XP_024309703.1:n.934-76A>T
NM_004453.4:c.1117-76A>T MANE Select	NP_004444.2:n.1117-76A>T
NM_001281737.2:c.976-76A>T	NP_001268666.1:n.976-76A>T