Canonical Allele Identifier: CA1239706426

Gene: HADHA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26204179C= , CM000664.2:g.26204179C=	GRCh38
NC_000002.11:g.26427048C= , CM000664.1:g.26427048C=	GRCh37
NC_000002.10:g.26280552C=	NCBI36
NG_007121.1:g.45442G=
NG_007121.2:g.45443G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1103G= MANE Select	ENSP00000370023.3:p.Gly368=
ENST00000492433.2:c.1103G=	ENSP00000438039.2:p.Gly368=
ENST00000643057.1:c.*994G=	ENSP00000493761.1:n.*994G=
ENST00000643063.1:c.*149G=	ENSP00000495353.1:n.*149G=
ENST00000643233.1:c.*994G=	ENSP00000493880.1:n.*994G=
ENST00000644428.1:c.1103G=	ENSP00000495560.1:p.Gly368=
ENST00000645274.1:c.998G=	ENSP00000493996.1:p.Gly333=
ENST00000646031.1:c.462G=
ENST00000646483.1:c.969G=	ENSP00000496185.1:n.969G=
ENST00000380649.7:c.1103G=	ENSP00000370023.3:p.Gly368=
NM_000182.4:c.1103G=	NP_000173.2:p.Gly368=
NM_000182.5:c.1103G= MANE Select	NP_000173.2:p.Gly368=