Canonical Allele Identifier: CA1239706453

Gene: HADHA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26204244_26204248delinsTTCAG , CM000664.2:g.26204244_26204248delinsTTCAG	GRCh38
NC_000002.11:g.26427113_26427117delinsTTCAG , CM000664.1:g.26427113_26427117delinsTTCAG	GRCh37
NC_000002.10:g.26280617_26280621delinsTTCAG	NCBI36
NG_007121.1:g.45373_45377delinsCTGAA
NG_007121.2:g.45374_45378delinsCTGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1086-52_1086-48delinsCTGAA MANE Select	ENSP00000370023.3:n.1086-52_1086-48delinsCTGAA
ENST00000492433.2:c.1086-52_1086-48delinsCTGAA	ENSP00000438039.2:n.1086-52_1086-48delinsCTGAA
ENST00000643057.1:c.*977-52_*977-48delinsCTGAA	ENSP00000493761.1:n.*977-52_*977-48delinsCTGAA
ENST00000643063.1:c.*132-52_*132-48delinsCTGAA	ENSP00000495353.1:n.*132-52_*132-48delinsCTGAA
ENST00000643233.1:c.*977-52_*977-48delinsCTGAA	ENSP00000493880.1:n.*977-52_*977-48delinsCTGAA
ENST00000644428.1:c.1086-52_1086-48delinsCTGAA	ENSP00000495560.1:n.1086-52_1086-48delinsCTGAA
ENST00000645274.1:c.981-52_981-48delinsCTGAA	ENSP00000493996.1:n.981-52_981-48delinsCTGAA
ENST00000646031.1:c.445-52_445-48delinsCTGAA
ENST00000646483.1:c.952-52_952-48delinsCTGAA	ENSP00000496185.1:n.952-52_952-48delinsCTGAA
ENST00000380649.7:c.1086-52_1086-48delinsCTGAA	ENSP00000370023.3:n.1086-52_1086-48delinsCTGAA
NM_000182.4:c.1086-52_1086-48delinsCTGAA	NP_000173.2:n.1086-52_1086-48delinsCTGAA
NM_000182.5:c.1086-52_1086-48delinsCTGAA MANE Select	NP_000173.2:n.1086-52_1086-48delinsCTGAA