Canonical Allele Identifier: CA1239700752

Gene: HADHA GAREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191270T= , CM000664.2:g.26191270T=	GRCh38
NC_000002.11:g.26414139T= , CM000664.1:g.26414139T=	GRCh37
NC_000002.10:g.26267643T=	NCBI36
NG_007121.1:g.58351A=
NG_007121.2:g.58352A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.2272A= (HADHA) MANE Select	ENSP00000370023.3:p.Asn758=
ENST00000492433.2:c.2359A= (HADHA)	ENSP00000438039.2:p.Asn787=
ENST00000643057.1:c.*2250A= (HADHA)	ENSP00000493761.1:n.*2250A=
ENST00000643063.1:c.*1318A= (HADHA)	ENSP00000495353.1:n.*1318A=
ENST00000643233.1:c.*2163A= (HADHA)	ENSP00000493880.1:n.*2163A=
ENST00000644428.1:c.*896A= (HADHA)	ENSP00000495560.1:n.*896A=
ENST00000645274.1:c.2167A= (HADHA)	ENSP00000493996.1:p.Asn723=
ENST00000646031.1:c.1631A= (HADHA)
ENST00000646483.1:c.2138A= (HADHA)	ENSP00000496185.1:n.2138A=
ENST00000380649.7:c.2272A= (HADHA)	ENSP00000370023.3:p.Asn758=
NM_000182.4:c.2272A= (HADHA)	NP_000173.2:p.Asn758=
XM_011532567.1:c.1683+3955T= (GAREM2)	XP_011530869.1:n.1683+3955T=
XM_011532567.3:c.1683+3955T= (GAREM2)	XP_011530869.1:n.1683+3955T=
NM_000182.5:c.2272A= (HADHA) MANE Select	NP_000173.2:p.Asn758=