Canonical Allele Identifier: CA346129973
Gene: HADHA HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000380649.8:c.1091T>C MANE Select ENSP00000370023.3:p.Leu364Pro
ENST00000492433.2:c.1091T>C ENSP00000438039.2:p.Leu364Pro
ENST00000643057.1:c.*982T>C ENSP00000493761.1:n.*982T>C
ENST00000643063.1:c.*137T>C ENSP00000495353.1:n.*137T>C
ENST00000643233.1:c.*982T>C ENSP00000493880.1:n.*982T>C
ENST00000644428.1:c.1091T>C ENSP00000495560.1:p.Leu364Pro
ENST00000645274.1:c.986T>C ENSP00000493996.1:p.Leu329Pro
ENST00000646031.1:c.450T>C
ENST00000646483.1:c.957T>C ENSP00000496185.1:n.957T>C
ENST00000380649.7:c.1091T>C ENSP00000370023.3:p.Leu364Pro
NM_000182.4:c.1091T>C NP_000173.2:p.Leu364Pro
NM_000182.5:c.1091T>C MANE Select NP_000173.2:p.Leu364Pro