Canonical Allele Identifier: CA425357850
Gene: HADHA HGNC NCBI
GAREM2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.26414188T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26191319T>A , CM000664.2:g.26191319T>A GRCh38
NC_000002.11:g.26414188T>A , CM000664.1:g.26414188T>A GRCh37
NC_000002.10:g.26267692T>A NCBI36
NG_007121.1:g.58302A>T
NG_007121.2:g.58303A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380649.8:c.2223A>T (HADHA) MANE Select ENSP00000370023.3:p.Gly741=
ENST00000492433.2:c.2310A>T (HADHA) ENSP00000438039.2:p.Gly770=
ENST00000643057.1:c.*2201A>T (HADHA) ENSP00000493761.1:n.*2201A>T
ENST00000643063.1:c.*1269A>T (HADHA) ENSP00000495353.1:n.*1269A>T
ENST00000643233.1:c.*2114A>T (HADHA) ENSP00000493880.1:n.*2114A>T
ENST00000644428.1:c.*847A>T (HADHA) ENSP00000495560.1:n.*847A>T
ENST00000645274.1:c.2118A>T (HADHA) ENSP00000493996.1:p.Gly706=
ENST00000646031.1:c.1582A>T (HADHA)
ENST00000646483.1:c.2089A>T (HADHA) ENSP00000496185.1:n.2089A>T
ENST00000380649.7:c.2223A>T (HADHA) ENSP00000370023.3:p.Gly741=
NM_000182.4:c.2223A>T (HADHA) NP_000173.2:p.Gly741=
XM_011532567.1:c.1683+4004T>A (GAREM2) XP_011530869.1:n.1683+4004T>A
XM_011532567.3:c.1683+4004T>A (GAREM2) XP_011530869.1:n.1683+4004T>A
NM_000182.5:c.2223A>T (HADHA) MANE Select NP_000173.2:p.Gly741=