Canonical Allele Identifier: CA1239702499
Gene: HADHA HGNC NCBI
GAREM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26195039A= , CM000664.2:g.26195039A= GRCh38
NC_000002.11:g.26417908A= , CM000664.1:g.26417908A= GRCh37
NC_000002.10:g.26271412A= NCBI36
NG_007121.1:g.54582T=
NG_007121.2:g.54583T=

Transcript Alleles

HGVS Amino-acid change
ENST00000380649.8:c.1620+53T= (HADHA) MANE Select ENSP00000370023.3:n.1620+53T=
ENST00000492433.2:c.1620+53T= (HADHA) ENSP00000438039.2:n.1620+53T=
ENST00000643057.1:c.*1511+53T= (HADHA) ENSP00000493761.1:n.*1511+53T=
ENST00000643063.1:c.*666+53T= (HADHA) ENSP00000495353.1:n.*666+53T=
ENST00000643233.1:c.*1511+53T= (HADHA) ENSP00000493880.1:n.*1511+53T=
ENST00000644428.1:c.*244+53T= (HADHA) ENSP00000495560.1:n.*244+53T=
ENST00000645274.1:c.1515+53T= (HADHA) ENSP00000493996.1:n.1515+53T=
ENST00000646031.1:c.979+53T= (HADHA)
ENST00000646483.1:c.1486+53T= (HADHA) ENSP00000496185.1:n.1486+53T=
ENST00000380649.7:c.1620+53T= (HADHA) ENSP00000370023.3:n.1620+53T=
ENST00000492433.1:c.78+53T= (HADHA) ENSP00000438039.1:n.78+53T=
NM_000182.4:c.1620+53T= (HADHA) NP_000173.2:n.1620+53T=
XM_011532567.1:c.1684-7194A= (GAREM2) XP_011530869.1:n.1684-7194A=
XM_011532567.3:c.1684-7194A= (GAREM2) XP_011530869.1:n.1684-7194A=
NM_000182.5:c.1620+53T= (HADHA) MANE Select NP_000173.2:n.1620+53T=