Canonical Allele Identifier: CA1239701238
Gene: HADHA HGNC NCBI
GAREM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26192310A= , CM000664.2:g.26192310A= GRCh38
NC_000002.11:g.26415179A= , CM000664.1:g.26415179A= GRCh37
NC_000002.10:g.26268683A= NCBI36
NG_007121.1:g.57311T=
NG_007121.2:g.57312T=

Transcript Alleles

HGVS Amino-acid change
ENST00000380649.8:c.2000T= (HADHA) MANE Select ENSP00000370023.3:p.Val667=
ENST00000492433.2:c.2000T= (HADHA) ENSP00000438039.2:p.Val667=
ENST00000643057.1:c.*1891T= (HADHA) ENSP00000493761.1:n.*1891T=
ENST00000643063.1:c.*1046T= (HADHA) ENSP00000495353.1:n.*1046T=
ENST00000643233.1:c.*1891T= (HADHA) ENSP00000493880.1:n.*1891T=
ENST00000644428.1:c.*624T= (HADHA) ENSP00000495560.1:n.*624T=
ENST00000645274.1:c.1895T= (HADHA) ENSP00000493996.1:p.Val632=
ENST00000646031.1:c.1359T= (HADHA)
ENST00000646483.1:c.1866T= (HADHA) ENSP00000496185.1:n.1866T=
ENST00000380649.7:c.2000T= (HADHA) ENSP00000370023.3:p.Val667=
ENST00000492433.1:c.458T= (HADHA) ENSP00000438039.1:p.Val153=
NM_000182.4:c.2000T= (HADHA) NP_000173.2:p.Val667=
XM_011532567.1:c.1683+4995A= (GAREM2) XP_011530869.1:n.1683+4995A=
XM_011532567.3:c.1683+4995A= (GAREM2) XP_011530869.1:n.1683+4995A=
NM_000182.5:c.2000T= (HADHA) MANE Select NP_000173.2:p.Val667=