Canonical Allele Identifier: CA358575617

Gene: ETFDH

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158685220G>T , CM000666.2:g.158685220G>T	GRCh38
NC_000004.11:g.159606372G>T , CM000666.1:g.159606372G>T	GRCh37
NC_000004.10:g.159825822G>T	NCBI36
NG_007078.2:g.17879G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004453.4:c.606+1G>T MANE Select	NP_004444.2:n.606+1G>T
ENST00000511912.6:c.606+1G>T MANE Select	ENSP00000426638.1:n.606+1G>T
NM_001281737.1:c.465+1G>T	NP_001268666.1:n.465+1G>T
NM_001281737.2:c.465+1G>T	NP_001268666.1:n.465+1G>T
NM_001281738.1:c.423+1G>T	NP_001268667.1:n.423+1G>T
NM_004453.3:c.606+1G>T	NP_004444.2:n.606+1G>T
ENST00000307738.5:c.465+1G>T	ENSP00000303552.5:n.465+1G>T
ENST00000506422.1:n.86+12730G>T
ENST00000507475.5:c.111+1G>T	ENSP00000422735.1:n.111+1G>T
ENST00000507475.6:n.379+1G>T
ENST00000511912.5:c.606+1G>T	ENSP00000426638.1:n.606+1G>T
ENST00000681978.1:n.855+1G>T
ENST00000682178.1:n.1638+1G>T
ENST00000682345.1:c.*306+547G>T	ENSP00000508122.1:n.*306+547G>T
ENST00000682452.1:n.937+1G>T
ENST00000682456.1:c.606+1G>T	ENSP00000508240.1:n.606+1G>T
ENST00000682601.1:n.797+1G>T
ENST00000682734.1:c.-568+547G>T	ENSP00000507860.1:n.-568+547G>T
ENST00000682820.1:n.643+1G>T
ENST00000682910.1:n.913+1G>T
ENST00000683004.1:c.*443+1G>T	ENSP00000506936.1:n.*443+1G>T
ENST00000683079.1:c.487+547G>T	ENSP00000507296.1:n.487+547G>T
ENST00000683081.1:c.*443+1G>T	ENSP00000507722.1:n.*443+1G>T
ENST00000683123.1:n.656G>T
ENST00000683305.1:c.423+1G>T	ENSP00000508043.1:n.423+1G>T
ENST00000683448.1:c.111+1G>T	ENSP00000506931.1:n.111+1G>T
ENST00000683478.1:c.487+547G>T	ENSP00000507793.1:n.487+547G>T
ENST00000683483.1:c.606+1G>T	ENSP00000507719.1:n.606+1G>T
ENST00000683750.1:n.729+1G>T
ENST00000683751.1:c.111+1G>T	ENSP00000506944.1:n.111+1G>T
ENST00000684036.1:c.423+1G>T	ENSP00000507276.1:n.423+1G>T
ENST00000684129.1:c.-613+547G>T	ENSP00000507174.1:n.-613+547G>T
ENST00000684209.1:n.846+1G>T
ENST00000684296.1:c.606+1G>T	ENSP00000507740.1:n.606+1G>T
ENST00000684505.1:c.555+1G>T	ENSP00000508237.1:n.555+1G>T
ENST00000684552.1:c.606+1G>T	ENSP00000506899.1:n.606+1G>T
ENST00000684611.1:n.2334+1G>T
ENST00000684622.1:c.606+1G>T	ENSP00000507546.1:n.606+1G>T
ENST00000684627.1:c.423+1G>T	ENSP00000507471.1:n.423+1G>T
ENST00000684641.1:c.606+1G>T	ENSP00000507642.1:n.606+1G>T
ENST00000684675.1:c.606+1G>T	ENSP00000506934.1:n.606+1G>T
ENST00000684749.1:n.675+1G>T
XM_024453935.1:c.423+1G>T	XP_024309703.1:n.423+1G>T