Canonical Allele Identifier: CA2658214878
Gene: HADHA HGNC NCBI
GAREM2 HGNC NCBI

Linked Data

gnomAD v4: 2-26191241-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26191241G>A , CM000664.2:g.26191241G>A GRCh38
NC_000002.11:g.26414110G>A , CM000664.1:g.26414110G>A GRCh37
NC_000002.10:g.26267614G>A NCBI36
NG_007121.1:g.58380C>T
NG_007121.2:g.58381C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380649.8:c.*9C>T (HADHA) MANE Select ENSP00000370023.3:n.*9C>T
ENST00000492433.2:c.*9C>T (HADHA) ENSP00000438039.2:n.*9C>T
ENST00000643057.1:c.*2279C>T (HADHA) ENSP00000493761.1:n.*2279C>T
ENST00000643063.1:c.*1347C>T (HADHA) ENSP00000495353.1:n.*1347C>T
ENST00000643233.1:c.*2192C>T (HADHA) ENSP00000493880.1:n.*2192C>T
ENST00000644428.1:c.*925C>T (HADHA) ENSP00000495560.1:n.*925C>T
ENST00000645274.1:c.*9C>T (HADHA) ENSP00000493996.1:n.*9C>T
ENST00000646031.1:c.1660C>T (HADHA)
ENST00000380649.7:c.*9C>T (HADHA) ENSP00000370023.3:n.*9C>T
NM_000182.4:c.*9C>T (HADHA) NP_000173.2:n.*9C>T
XM_011532567.1:c.1683+3926G>A (GAREM2) XP_011530869.1:n.1683+3926G>A
XM_011532567.3:c.1683+3926G>A (GAREM2) XP_011530869.1:n.1683+3926G>A
NM_000182.5:c.*9C>T (HADHA) MANE Select NP_000173.2:n.*9C>T