Canonical Allele Identifier: CA1239701230
Gene: HADHA HGNC NCBI
GAREM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26192297C= , CM000664.2:g.26192297C= GRCh38
NC_000002.11:g.26415166C= , CM000664.1:g.26415166C= GRCh37
NC_000002.10:g.26268670C= NCBI36
NG_007121.1:g.57324G=
NG_007121.2:g.57325G=

Transcript Alleles

HGVS Amino-acid change
ENST00000380649.8:c.2000+13G= (HADHA) MANE Select ENSP00000370023.3:n.2000+13G=
ENST00000492433.2:c.2000+13G= (HADHA) ENSP00000438039.2:n.2000+13G=
ENST00000643057.1:c.*1891+13G= (HADHA) ENSP00000493761.1:n.*1891+13G=
ENST00000643063.1:c.*1046+13G= (HADHA) ENSP00000495353.1:n.*1046+13G=
ENST00000643233.1:c.*1891+13G= (HADHA) ENSP00000493880.1:n.*1891+13G=
ENST00000644428.1:c.*624+13G= (HADHA) ENSP00000495560.1:n.*624+13G=
ENST00000645274.1:c.1895+13G= (HADHA) ENSP00000493996.1:n.1895+13G=
ENST00000646031.1:c.1359+13G= (HADHA)
ENST00000646483.1:c.1866+13G= (HADHA) ENSP00000496185.1:n.1866+13G=
ENST00000380649.7:c.2000+13G= (HADHA) ENSP00000370023.3:n.2000+13G=
ENST00000492433.1:c.458+13G= (HADHA) ENSP00000438039.1:n.458+13G=
NM_000182.4:c.2000+13G= (HADHA) NP_000173.2:n.2000+13G=
XM_011532567.1:c.1683+4982C= (GAREM2) XP_011530869.1:n.1683+4982C=
XM_011532567.3:c.1683+4982C= (GAREM2) XP_011530869.1:n.1683+4982C=
NM_000182.5:c.2000+13G= (HADHA) MANE Select NP_000173.2:n.2000+13G=