Canonical Allele Identifier: CA2658214733
Gene: HADHA HGNC NCBI
GAREM2 HGNC NCBI

Linked Data

gnomAD v4: 2-26191180-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26191180A>G , CM000664.2:g.26191180A>G GRCh38
NC_000002.11:g.26414049A>G , CM000664.1:g.26414049A>G GRCh37
NC_000002.10:g.26267553A>G NCBI36
NG_007121.1:g.58441T>C
NG_007121.2:g.58442T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380649.8:c.*70T>C (HADHA) MANE Select ENSP00000370023.3:n.*70T>C
ENST00000492433.2:c.*70T>C (HADHA) ENSP00000438039.2:n.*70T>C
ENST00000643057.1:c.*2340T>C (HADHA) ENSP00000493761.1:n.*2340T>C
ENST00000643063.1:c.*1408T>C (HADHA) ENSP00000495353.1:n.*1408T>C
ENST00000643233.1:c.*2253T>C (HADHA) ENSP00000493880.1:n.*2253T>C
ENST00000644428.1:c.*986T>C (HADHA) ENSP00000495560.1:n.*986T>C
ENST00000645274.1:c.*70T>C (HADHA) ENSP00000493996.1:n.*70T>C
ENST00000646031.1:c.1721T>C (HADHA)
ENST00000380649.7:c.*70T>C (HADHA) ENSP00000370023.3:n.*70T>C
NM_000182.4:c.*70T>C (HADHA) NP_000173.2:n.*70T>C
XM_011532567.1:c.1683+3865A>G (GAREM2) XP_011530869.1:n.1683+3865A>G
XM_011532567.3:c.1683+3865A>G (GAREM2) XP_011530869.1:n.1683+3865A>G
NM_000182.5:c.*70T>C (HADHA) MANE Select NP_000173.2:n.*70T>C