Canonical Allele Identifier: CA555632862
Gene: ETFDH HGNC NCBI

Linked Data

dbSNP Id: rs1248954017

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.158680343_158680344del , CM000666.2:g.158680343_158680344del GRCh38
NC_000004.11:g.159601495_159601496del , CM000666.1:g.159601495_159601496del GRCh37
NC_000004.10:g.159820945_159820946del NCBI36
NG_007078.2:g.13002_13003del

Transcript Alleles

HGVS Amino-acid Change
ENST00000436096.3:n.286-124_286-123del
ENST00000507475.6:n.179-4249_179-4248del
ENST00000681978.1:n.160_161del
ENST00000682178.1:n.60-124_60-123del
ENST00000682345.1:c.35-185_35-184del ENSP00000508122.1:n.35-185_35-184del
ENST00000682409.1:n.144-124_144-123del
ENST00000682452.1:n.242_243del
ENST00000682456.1:c.35-124_35-123del ENSP00000508240.1:n.35-124_35-123del
ENST00000682601.1:n.226-124_226-123del
ENST00000682734.1:c.-649-4249_-649-4248del ENSP00000507860.1:n.-649-4249_-649-4248del
ENST00000682820.1:n.72-124_72-123del
ENST00000682910.1:n.218_219del
ENST00000683004.1:c.35-124_35-123del ENSP00000506936.1:n.35-124_35-123del
ENST00000683079.1:c.35-124_35-123del ENSP00000507296.1:n.35-124_35-123del
ENST00000683081.1:c.35-124_35-123del ENSP00000507722.1:n.35-124_35-123del
ENST00000683305.1:c.-52-1228_-52-1227del ENSP00000508043.1:n.-52-1228_-52-1227del
ENST00000683448.1:c.-90-4249_-90-4248del ENSP00000506931.1:n.-90-4249_-90-4248del
ENST00000683478.1:c.35-124_35-123del ENSP00000507793.1:n.35-124_35-123del
ENST00000683483.1:c.35-124_35-123del ENSP00000507719.1:n.35-124_35-123del
ENST00000683750.1:n.158-124_158-123del
ENST00000683751.1:c.-90-4249_-90-4248del ENSP00000506944.1:n.-90-4249_-90-4248del
ENST00000683799.1:n.220_221del
ENST00000684036.1:c.-149-124_-149-123del ENSP00000507276.1:n.-149-124_-149-123del
ENST00000684129.1:c.-694-4249_-694-4248del ENSP00000507174.1:n.-694-4249_-694-4248del
ENST00000684209.1:n.151_152del
ENST00000684296.1:c.35-124_35-123del ENSP00000507740.1:n.35-124_35-123del
ENST00000684505.1:c.35-124_35-123del ENSP00000508237.1:n.35-124_35-123del
ENST00000684552.1:c.35-124_35-123del ENSP00000506899.1:n.35-124_35-123del
ENST00000684611.1:n.176-124_176-123del
ENST00000684622.1:c.35-124_35-123del ENSP00000507546.1:n.35-124_35-123del
ENST00000684627.1:c.-149-124_-149-123del ENSP00000507471.1:n.-149-124_-149-123del
ENST00000684641.1:c.35-124_35-123del ENSP00000507642.1:n.35-124_35-123del
ENST00000684675.1:c.35-124_35-123del ENSP00000506934.1:n.35-124_35-123del
ENST00000684749.1:n.60-124_60-123del
ENST00000511912.6:c.35-124_35-123del MANE Select ENSP00000426638.1:n.35-124_35-123del
ENST00000307738.5:c.35-1852_35-1851del ENSP00000303552.5:n.35-1852_35-1851del
ENST00000436096.2:n.176-124_176-123del
ENST00000506422.1:n.86+7853_86+7854del
ENST00000507475.5:c.-90-4249_-90-4248del ENSP00000422735.1:n.-90-4249_-90-4248del
ENST00000511912.5:c.35-124_35-123del ENSP00000426638.1:n.35-124_35-123del
ENST00000512251.5:c.35-185_35-184del ENSP00000425661.1:n.35-185_35-184del
NM_001281737.1:c.35-1852_35-1851del NP_001268666.1:n.35-1852_35-1851del
NM_004453.3:c.35-124_35-123del NP_004444.2:n.35-124_35-123del
XM_024453935.1:c.-149-124_-149-123del XP_024309703.1:n.-149-124_-149-123del
NM_004453.4:c.35-124_35-123del MANE Select NP_004444.2:n.35-124_35-123del
NM_001281737.2:c.35-1852_35-1851del NP_001268666.1:n.35-1852_35-1851del