Canonical Allele Identifier: CA1239706385

Gene: HADHA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26204073T= , CM000664.2:g.26204073T=	GRCh38
NC_000002.11:g.26426942T= , CM000664.1:g.26426942T=	GRCh37
NC_000002.10:g.26280446T=	NCBI36
NG_007121.1:g.45548A=
NG_007121.2:g.45549A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1209A= MANE Select	ENSP00000370023.3:p.Gln403=
ENST00000492433.2:c.1209A=	ENSP00000438039.2:p.Gln403=
ENST00000643057.1:c.*1100A=	ENSP00000493761.1:n.*1100A=
ENST00000643063.1:c.*255A=	ENSP00000495353.1:n.*255A=
ENST00000643233.1:c.*1100A=	ENSP00000493880.1:n.*1100A=
ENST00000644428.1:c.1209A=	ENSP00000495560.1:p.Gln403=
ENST00000645274.1:c.1104A=	ENSP00000493996.1:p.Gln368=
ENST00000646031.1:c.568A=
ENST00000646483.1:c.1075A=	ENSP00000496185.1:n.1075A=
ENST00000380649.7:c.1209A=	ENSP00000370023.3:p.Gln403=
NM_000182.4:c.1209A=	NP_000173.2:p.Gln403=
NM_000182.5:c.1209A= MANE Select	NP_000173.2:p.Gln403=