Canonical Allele Identifier: CA1239700730

Gene: HADHA GAREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191224C= , CM000664.2:g.26191224C=	GRCh38
NC_000002.11:g.26414093C= , CM000664.1:g.26414093C=	GRCh37
NC_000002.10:g.26267597C=	NCBI36
NG_007121.1:g.58397G=
NG_007121.2:g.58398G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.*26G= (HADHA) MANE Select	ENSP00000370023.3:n.*26G=
ENST00000492433.2:c.*26G= (HADHA)	ENSP00000438039.2:n.*26G=
ENST00000643057.1:c.*2296G= (HADHA)	ENSP00000493761.1:n.*2296G=
ENST00000643063.1:c.*1364G= (HADHA)	ENSP00000495353.1:n.*1364G=
ENST00000643233.1:c.*2209G= (HADHA)	ENSP00000493880.1:n.*2209G=
ENST00000644428.1:c.*942G= (HADHA)	ENSP00000495560.1:n.*942G=
ENST00000645274.1:c.*26G= (HADHA)	ENSP00000493996.1:n.*26G=
ENST00000646031.1:c.1677G= (HADHA)
ENST00000380649.7:c.*26G= (HADHA)	ENSP00000370023.3:n.*26G=
NM_000182.4:c.*26G= (HADHA)	NP_000173.2:n.*26G=
XM_011532567.1:c.1683+3909C= (GAREM2)	XP_011530869.1:n.1683+3909C=
XM_011532567.3:c.1683+3909C= (GAREM2)	XP_011530869.1:n.1683+3909C=
NM_000182.5:c.*26G= (HADHA) MANE Select	NP_000173.2:n.*26G=