Canonical Allele Identifier: CA1559356
Gene: HADHA HGNC NCBI
GAREM2 HGNC NCBI

Linked Data

dbSNP Id: rs778131571
gnomAD v2: 2-26414323-G-A
gnomAD v4: 2-26191454-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26191454G>A , CM000664.2:g.26191454G>A GRCh38
NC_000002.11:g.26414323G>A , CM000664.1:g.26414323G>A GRCh37
NC_000002.10:g.26267827G>A NCBI36
NG_007121.1:g.58167C>T
NG_007121.2:g.58168C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380649.8:c.2146+29C>T (HADHA) MANE Select ENSP00000370023.3:n.2146+29C>T
ENST00000492433.2:c.2175C>T (HADHA) ENSP00000438039.2:p.Leu725=
ENST00000643057.1:c.*2066C>T (HADHA) ENSP00000493761.1:n.*2066C>T
ENST00000643063.1:c.*1192+29C>T (HADHA) ENSP00000495353.1:n.*1192+29C>T
ENST00000643233.1:c.*2037+29C>T (HADHA) ENSP00000493880.1:n.*2037+29C>T
ENST00000644428.1:c.*770+29C>T (HADHA) ENSP00000495560.1:n.*770+29C>T
ENST00000645274.1:c.2041+29C>T (HADHA) ENSP00000493996.1:n.2041+29C>T
ENST00000646031.1:c.1505+29C>T (HADHA)
ENST00000646483.1:c.2012+29C>T (HADHA) ENSP00000496185.1:n.2012+29C>T
ENST00000380649.7:c.2146+29C>T (HADHA) ENSP00000370023.3:n.2146+29C>T
ENST00000492433.1:c.633C>T (HADHA) ENSP00000438039.1:p.Leu211=
NM_000182.4:c.2146+29C>T (HADHA) NP_000173.2:n.2146+29C>T
XM_011532567.1:c.1683+4139G>A (GAREM2) XP_011530869.1:n.1683+4139G>A
XM_011532567.3:c.1683+4139G>A (GAREM2) XP_011530869.1:n.1683+4139G>A
NM_000182.5:c.2146+29C>T (HADHA) MANE Select NP_000173.2:n.2146+29C>T