Canonical Allele Identifier: CA346129227
Gene: HADHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26204126T>A , CM000664.2:g.26204126T>A GRCh38
NC_000002.11:g.26426995T>A , CM000664.1:g.26426995T>A GRCh37
NC_000002.10:g.26280499T>A NCBI36
NG_007121.1:g.45495A>T
NG_007121.2:g.45496A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380649.8:c.1156A>T MANE Select ENSP00000370023.3:p.Lys386Ter
ENST00000492433.2:c.1156A>T ENSP00000438039.2:p.Lys386Ter
ENST00000643057.1:c.*1047A>T ENSP00000493761.1:n.*1047A>T
ENST00000643063.1:c.*202A>T ENSP00000495353.1:n.*202A>T
ENST00000643233.1:c.*1047A>T ENSP00000493880.1:n.*1047A>T
ENST00000644428.1:c.1156A>T ENSP00000495560.1:p.Lys386Ter
ENST00000645274.1:c.1051A>T ENSP00000493996.1:p.Lys351Ter
ENST00000646031.1:c.515A>T
ENST00000646483.1:c.1022A>T ENSP00000496185.1:n.1022A>T
ENST00000380649.7:c.1156A>T ENSP00000370023.3:p.Lys386Ter
NM_000182.4:c.1156A>T NP_000173.2:p.Lys386Ter
NM_000182.5:c.1156A>T MANE Select NP_000173.2:p.Lys386Ter