Canonical Allele Identifier: CA2629647717
Gene: ETFA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.76274335G>T , CM000677.2:g.76274335G>T GRCh38
NC_000015.9:g.76566676G>T , CM000677.1:g.76566676G>T GRCh37
NC_000015.8:g.74353731G>T NCBI36
NG_007077.2:g.42135C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000559386.2:c.816+77C>A ENSP00000452777.2:n.816+77C>A
ENST00000560044.6:c.*811+77C>A ENSP00000452942.1:n.*811+77C>A
ENST00000560595.6:c.1035+77C>A ENSP00000453345.2:n.1035+77C>A
ENST00000565910.6:c.816+77C>A ENSP00000458001.2:n.816+77C>A
ENST00000685118.1:c.*811+77C>A ENSP00000509473.1:n.*811+77C>A
ENST00000685548.1:c.816+77C>A ENSP00000510343.1:n.816+77C>A
ENST00000685863.1:c.600+77C>A ENSP00000509361.1:n.600+77C>A
ENST00000687293.1:c.891+77C>A ENSP00000509928.1:n.891+77C>A
ENST00000687975.1:c.*692+77C>A ENSP00000508690.1:n.*692+77C>A
ENST00000688154.1:c.816+77C>A ENSP00000510637.1:n.816+77C>A
ENST00000688389.1:c.747+77C>A ENSP00000510491.1:n.747+77C>A
ENST00000688637.1:n.897+77C>A
ENST00000688908.1:c.651+77C>A ENSP00000510242.1:n.651+77C>A
ENST00000689730.1:c.798+77C>A ENSP00000510006.1:n.798+77C>A
ENST00000689739.1:n.828+77C>A
ENST00000690610.1:c.816+77C>A ENSP00000510473.1:n.816+77C>A
ENST00000691021.1:c.*811+77C>A ENSP00000510805.1:n.*811+77C>A
ENST00000691071.1:n.595+77C>A
ENST00000691695.1:c.669+77C>A ENSP00000509402.1:n.669+77C>A
ENST00000692691.1:c.939+77C>A ENSP00000508808.1:n.939+77C>A
ENST00000693064.1:c.*791+77C>A ENSP00000510720.1:n.*791+77C>A
ENST00000557943.6:c.816+77C>A MANE Select ENSP00000452762.1:n.816+77C>A
ENST00000267950.12:c.*539+77C>A ENSP00000267950.8:n.*539+77C>A
ENST00000433983.6:c.669+77C>A ENSP00000399273.2:n.669+77C>A
ENST00000557943.5:c.816+77C>A ENSP00000452762.1:n.816+77C>A
ENST00000558803.1:n.245C>A
ENST00000559075.5:n.840+77C>A
ENST00000559602.5:c.504+77C>A ENSP00000452659.1:n.504+77C>A
ENST00000559758.5:n.734C>A
ENST00000559973.5:c.526+77C>A
ENST00000560044.5:c.*811+77C>A ENSP00000452942.1:n.*811+77C>A
ENST00000560595.5:c.747+77C>A ENSP00000453345.1:n.747+77C>A
ENST00000560726.5:c.36+77C>A ENSP00000453098.1:n.36+77C>A
ENST00000560816.5:n.375+77C>A
ENST00000560899.5:c.36+77C>A ENSP00000453422.1:n.36+77C>A
NM_000126.3:c.816+77C>A NP_000117.1:n.816+77C>A
NM_001127716.1:c.669+77C>A NP_001121188.1:n.669+77C>A
XR_931766.1:n.871+77C>A
XR_931766.3:n.897+77C>A
NM_000126.4:c.816+77C>A MANE Select NP_000117.1:n.816+77C>A
NM_001127716.2:c.669+77C>A NP_001121188.1:n.669+77C>A