Canonical Allele Identifier: CA1239700762

Gene: HADHA GAREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191298C= , CM000664.2:g.26191298C=	GRCh38
NC_000002.11:g.26414167C= , CM000664.1:g.26414167C=	GRCh37
NC_000002.10:g.26267671C=	NCBI36
NG_007121.1:g.58323G=
NG_007121.2:g.58324G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.2244G= (HADHA) MANE Select	ENSP00000370023.3:p.Gln748=
ENST00000492433.2:c.2331G= (HADHA)	ENSP00000438039.2:p.Gln777=
ENST00000643057.1:c.*2222G= (HADHA)	ENSP00000493761.1:n.*2222G=
ENST00000643063.1:c.*1290G= (HADHA)	ENSP00000495353.1:n.*1290G=
ENST00000643233.1:c.*2135G= (HADHA)	ENSP00000493880.1:n.*2135G=
ENST00000644428.1:c.*868G= (HADHA)	ENSP00000495560.1:n.*868G=
ENST00000645274.1:c.2139G= (HADHA)	ENSP00000493996.1:p.Gln713=
ENST00000646031.1:c.1603G= (HADHA)
ENST00000646483.1:c.2110G= (HADHA)	ENSP00000496185.1:n.2110G=
ENST00000380649.7:c.2244G= (HADHA)	ENSP00000370023.3:p.Gln748=
NM_000182.4:c.2244G= (HADHA)	NP_000173.2:p.Gln748=
XM_011532567.1:c.1683+3983C= (GAREM2)	XP_011530869.1:n.1683+3983C=
XM_011532567.3:c.1683+3983C= (GAREM2)	XP_011530869.1:n.1683+3983C=
NM_000182.5:c.2244G= (HADHA) MANE Select	NP_000173.2:p.Gln748=