Canonical Allele Identifier: CA1239706395

Gene: HADHA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26204094C= , CM000664.2:g.26204094C=	GRCh38
NC_000002.11:g.26426963C= , CM000664.1:g.26426963C=	GRCh37
NC_000002.10:g.26280467C=	NCBI36
NG_007121.1:g.45527G=
NG_007121.2:g.45528G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1188G= MANE Select	ENSP00000370023.3:p.Ala396=
ENST00000492433.2:c.1188G=	ENSP00000438039.2:p.Ala396=
ENST00000643057.1:c.*1079G=	ENSP00000493761.1:n.*1079G=
ENST00000643063.1:c.*234G=	ENSP00000495353.1:n.*234G=
ENST00000643233.1:c.*1079G=	ENSP00000493880.1:n.*1079G=
ENST00000644428.1:c.1188G=	ENSP00000495560.1:p.Ala396=
ENST00000645274.1:c.1083G=	ENSP00000493996.1:p.Ala361=
ENST00000646031.1:c.547G=
ENST00000646483.1:c.1054G=	ENSP00000496185.1:n.1054G=
ENST00000380649.7:c.1188G=	ENSP00000370023.3:p.Ala396=
NM_000182.4:c.1188G=	NP_000173.2:p.Ala396=
NM_000182.5:c.1188G= MANE Select	NP_000173.2:p.Ala396=