Canonical Allele Identifier: CA425201522

Gene: HADHA

Linked Data

• MyVariant Identifiers: chr2:g.26427041C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26204172C>A , CM000664.2:g.26204172C>A	GRCh38
NC_000002.11:g.26427041C>A , CM000664.1:g.26427041C>A	GRCh37
NC_000002.10:g.26280545C>A	NCBI36
NG_007121.1:g.45449G>T
NG_007121.2:g.45450G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1110G>T MANE Select	ENSP00000370023.3:p.Gly370=
ENST00000492433.2:c.1110G>T	ENSP00000438039.2:p.Gly370=
ENST00000643057.1:c.*1001G>T	ENSP00000493761.1:n.*1001G>T
ENST00000643063.1:c.*156G>T	ENSP00000495353.1:n.*156G>T
ENST00000643233.1:c.*1001G>T	ENSP00000493880.1:n.*1001G>T
ENST00000644428.1:c.1110G>T	ENSP00000495560.1:p.Gly370=
ENST00000645274.1:c.1005G>T	ENSP00000493996.1:p.Gly335=
ENST00000646031.1:c.469G>T
ENST00000646483.1:c.976G>T	ENSP00000496185.1:n.976G>T
ENST00000380649.7:c.1110G>T	ENSP00000370023.3:p.Gly370=
NM_000182.4:c.1110G>T	NP_000173.2:p.Gly370=
NM_000182.5:c.1110G>T MANE Select	NP_000173.2:p.Gly370=