Canonical Allele Identifier: CA346128780

Gene: HADHA

Linked Data

• MyVariant Identifiers: chr2:g.26426959C>A (hg19) ; chr2:g.26204090C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26204090C>A , CM000664.2:g.26204090C>A	GRCh38
NC_000002.11:g.26426959C>A , CM000664.1:g.26426959C>A	GRCh37
NC_000002.10:g.26280463C>A	NCBI36
NG_007121.1:g.45531G>T
NG_007121.2:g.45532G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1192G>T MANE Select	ENSP00000370023.3:p.Asp398Tyr
ENST00000492433.2:c.1192G>T	ENSP00000438039.2:p.Asp398Tyr
ENST00000643057.1:c.*1083G>T	ENSP00000493761.1:n.*1083G>T
ENST00000643063.1:c.*238G>T	ENSP00000495353.1:n.*238G>T
ENST00000643233.1:c.*1083G>T	ENSP00000493880.1:n.*1083G>T
ENST00000644428.1:c.1192G>T	ENSP00000495560.1:p.Asp398Tyr
ENST00000645274.1:c.1087G>T	ENSP00000493996.1:p.Asp363Tyr
ENST00000646031.1:c.551G>T
ENST00000646483.1:c.1058G>T	ENSP00000496185.1:n.1058G>T
ENST00000380649.7:c.1192G>T	ENSP00000370023.3:p.Asp398Tyr
NM_000182.4:c.1192G>T	NP_000173.2:p.Asp398Tyr
NM_000182.5:c.1192G>T MANE Select	NP_000173.2:p.Asp398Tyr