Canonical Allele Identifier: CA2658214702
Gene: HADHA HGNC NCBI
GAREM2 HGNC NCBI

Linked Data

gnomAD v4: 2-26191156-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26191156G>T , CM000664.2:g.26191156G>T GRCh38
NC_000002.11:g.26414025G>T , CM000664.1:g.26414025G>T GRCh37
NC_000002.10:g.26267529G>T NCBI36
NG_007121.1:g.58465C>A
NG_007121.2:g.58466C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380649.8:c.*94C>A (HADHA) MANE Select ENSP00000370023.3:n.*94C>A
ENST00000492433.2:c.*94C>A (HADHA) ENSP00000438039.2:n.*94C>A
ENST00000643057.1:c.*2364C>A (HADHA) ENSP00000493761.1:n.*2364C>A
ENST00000643063.1:c.*1432C>A (HADHA) ENSP00000495353.1:n.*1432C>A
ENST00000643233.1:c.*2277C>A (HADHA) ENSP00000493880.1:n.*2277C>A
ENST00000644428.1:c.*1010C>A (HADHA) ENSP00000495560.1:n.*1010C>A
ENST00000645274.1:c.*94C>A (HADHA) ENSP00000493996.1:n.*94C>A
ENST00000646031.1:c.1745C>A (HADHA)
ENST00000380649.7:c.*94C>A (HADHA) ENSP00000370023.3:n.*94C>A
NM_000182.4:c.*94C>A (HADHA) NP_000173.2:n.*94C>A
XM_011532567.1:c.1683+3841G>T (GAREM2) XP_011530869.1:n.1683+3841G>T
XM_011532567.3:c.1683+3841G>T (GAREM2) XP_011530869.1:n.1683+3841G>T
NM_000182.5:c.*94C>A (HADHA) MANE Select NP_000173.2:n.*94C>A