Canonical Allele Identifier: CA346129979

Gene: HADHA

Linked Data

• MyVariant Identifiers: chr2:g.26427060A>T (hg19) ; chr2:g.26204191A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26204191A>T , CM000664.2:g.26204191A>T	GRCh38
NC_000002.11:g.26427060A>T , CM000664.1:g.26427060A>T	GRCh37
NC_000002.10:g.26280564A>T	NCBI36
NG_007121.1:g.45430T>A
NG_007121.2:g.45431T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1091T>A MANE Select	ENSP00000370023.3:p.Leu364Gln
ENST00000492433.2:c.1091T>A	ENSP00000438039.2:p.Leu364Gln
ENST00000643057.1:c.*982T>A	ENSP00000493761.1:n.*982T>A
ENST00000643063.1:c.*137T>A	ENSP00000495353.1:n.*137T>A
ENST00000643233.1:c.*982T>A	ENSP00000493880.1:n.*982T>A
ENST00000644428.1:c.1091T>A	ENSP00000495560.1:p.Leu364Gln
ENST00000645274.1:c.986T>A	ENSP00000493996.1:p.Leu329Gln
ENST00000646031.1:c.450T>A
ENST00000646483.1:c.957T>A	ENSP00000496185.1:n.957T>A
ENST00000380649.7:c.1091T>A	ENSP00000370023.3:p.Leu364Gln
NM_000182.4:c.1091T>A	NP_000173.2:p.Leu364Gln
NM_000182.5:c.1091T>A MANE Select	NP_000173.2:p.Leu364Gln