Canonical Allele Identifier: CA346128725

Gene: HADHA

Linked Data

• MyVariant Identifiers: chr2:g.26426950G>C (hg19) ; chr2:g.26204081G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26204081G>C , CM000664.2:g.26204081G>C	GRCh38
NC_000002.11:g.26426950G>C , CM000664.1:g.26426950G>C	GRCh37
NC_000002.10:g.26280454G>C	NCBI36
NG_007121.1:g.45540C>G
NG_007121.2:g.45541C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000380649.8:c.1201C>G MANE Select	ENSP00000370023.3:p.Gln401Glu
ENST00000492433.2:c.1201C>G	ENSP00000438039.2:p.Gln401Glu
ENST00000643057.1:c.*1092C>G	ENSP00000493761.1:n.*1092C>G
ENST00000643063.1:c.*247C>G	ENSP00000495353.1:n.*247C>G
ENST00000643233.1:c.*1092C>G	ENSP00000493880.1:n.*1092C>G
ENST00000644428.1:c.1201C>G	ENSP00000495560.1:p.Gln401Glu
ENST00000645274.1:c.1096C>G	ENSP00000493996.1:p.Gln366Glu
ENST00000646031.1:c.560C>G
ENST00000646483.1:c.1067C>G	ENSP00000496185.1:n.1067C>G
ENST00000380649.7:c.1201C>G	ENSP00000370023.3:p.Gln401Glu
NM_000182.4:c.1201C>G	NP_000173.2:p.Gln401Glu
NM_000182.5:c.1201C>G MANE Select	NP_000173.2:p.Gln401Glu