Canonical Allele Identifier: CA1239720439

Gene: HADHA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26238843A= , CM000664.2:g.26238843A=	GRCh38
NC_000002.11:g.26461711A= , CM000664.1:g.26461711A=	GRCh37
NC_000002.10:g.26315215A=	NCBI36
NG_007121.1:g.10779T=
NG_007121.2:g.10779T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000380649.8:c.180+91T= MANE Select	ENSP00000370023.3:n.180+91T=
ENST00000471743.2:n.191+91T=
ENST00000492433.2:c.180+91T=	ENSP00000438039.2:n.180+91T=
ENST00000643057.1:c.*71+91T=	ENSP00000493761.1:n.*71+91T=
ENST00000643063.1:c.180+91T=	ENSP00000495353.1:n.180+91T=
ENST00000643233.1:c.*71+91T=	ENSP00000493880.1:n.*71+91T=
ENST00000644428.1:c.180+91T=	ENSP00000495560.1:n.180+91T=
ENST00000645274.1:c.180+91T=	ENSP00000493996.1:n.180+91T=
ENST00000646483.1:c.180+91T=	ENSP00000496185.1:n.180+91T=
ENST00000380649.7:c.180+91T=	ENSP00000370023.3:n.180+91T=
NM_000182.4:c.180+91T=	NP_000173.2:n.180+91T=
NM_000182.5:c.180+91T= MANE Select	NP_000173.2:n.180+91T=