Canonical Allele Identifier: CA346129024

Gene: HADHA

Linked Data

• MyVariant Identifiers: chr2:g.26426980C>A (hg19) ; chr2:g.26204111C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26204111C>A , CM000664.2:g.26204111C>A	GRCh38
NC_000002.11:g.26426980C>A , CM000664.1:g.26426980C>A	GRCh37
NC_000002.10:g.26280484C>A	NCBI36
NG_007121.1:g.45510G>T
NG_007121.2:g.45511G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1171G>T MANE Select	ENSP00000370023.3:p.Asp391Tyr
ENST00000492433.2:c.1171G>T	ENSP00000438039.2:p.Asp391Tyr
ENST00000643057.1:c.*1062G>T	ENSP00000493761.1:n.*1062G>T
ENST00000643063.1:c.*217G>T	ENSP00000495353.1:n.*217G>T
ENST00000643233.1:c.*1062G>T	ENSP00000493880.1:n.*1062G>T
ENST00000644428.1:c.1171G>T	ENSP00000495560.1:p.Asp391Tyr
ENST00000645274.1:c.1066G>T	ENSP00000493996.1:p.Asp356Tyr
ENST00000646031.1:c.530G>T
ENST00000646483.1:c.1037G>T	ENSP00000496185.1:n.1037G>T
ENST00000380649.7:c.1171G>T	ENSP00000370023.3:p.Asp391Tyr
NM_000182.4:c.1171G>T	NP_000173.2:p.Asp391Tyr
NM_000182.5:c.1171G>T MANE Select	NP_000173.2:p.Asp391Tyr