Canonical Allele Identifier: CA425201442

Gene: HADHA

Linked Data

• MyVariant Identifiers: chr2:g.26426996T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26204127T>C , CM000664.2:g.26204127T>C	GRCh38
NC_000002.11:g.26426996T>C , CM000664.1:g.26426996T>C	GRCh37
NC_000002.10:g.26280500T>C	NCBI36
NG_007121.1:g.45494A>G
NG_007121.2:g.45495A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1155A>G MANE Select	ENSP00000370023.3:p.Leu385=
ENST00000492433.2:c.1155A>G	ENSP00000438039.2:p.Leu385=
ENST00000643057.1:c.*1046A>G	ENSP00000493761.1:n.*1046A>G
ENST00000643063.1:c.*201A>G	ENSP00000495353.1:n.*201A>G
ENST00000643233.1:c.*1046A>G	ENSP00000493880.1:n.*1046A>G
ENST00000644428.1:c.1155A>G	ENSP00000495560.1:p.Leu385=
ENST00000645274.1:c.1050A>G	ENSP00000493996.1:p.Leu350=
ENST00000646031.1:c.514A>G
ENST00000646483.1:c.1021A>G	ENSP00000496185.1:n.1021A>G
ENST00000380649.7:c.1155A>G	ENSP00000370023.3:p.Leu385=
NM_000182.4:c.1155A>G	NP_000173.2:p.Leu385=
NM_000182.5:c.1155A>G MANE Select	NP_000173.2:p.Leu385=