Canonical Allele Identifier: CA2658205423

Gene: HADHA

Linked Data

• gnomAD v4: 2-26204267-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26204268_26204269del , CM000664.2:g.26204268_26204269del	GRCh38
NC_000002.11:g.26427137_26427138del , CM000664.1:g.26427137_26427138del	GRCh37
NC_000002.10:g.26280641_26280642del	NCBI36
NG_007121.1:g.45352_45353del
NG_007121.2:g.45353_45354del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1086-73_1086-72del MANE Select	ENSP00000370023.3:n.1086-73_1086-72del
ENST00000492433.2:c.1086-73_1086-72del	ENSP00000438039.2:n.1086-73_1086-72del
ENST00000643057.1:c.*977-73_*977-72del	ENSP00000493761.1:n.*977-73_*977-72del
ENST00000643063.1:c.*132-73_*132-72del	ENSP00000495353.1:n.*132-73_*132-72del
ENST00000643233.1:c.*977-73_*977-72del	ENSP00000493880.1:n.*977-73_*977-72del
ENST00000644428.1:c.1086-73_1086-72del	ENSP00000495560.1:n.1086-73_1086-72del
ENST00000645274.1:c.981-73_981-72del	ENSP00000493996.1:n.981-73_981-72del
ENST00000646031.1:c.445-73_445-72del
ENST00000646483.1:c.952-73_952-72del	ENSP00000496185.1:n.952-73_952-72del
ENST00000380649.7:c.1086-73_1086-72del	ENSP00000370023.3:n.1086-73_1086-72del
NM_000182.4:c.1086-73_1086-72del	NP_000173.2:n.1086-73_1086-72del
NM_000182.5:c.1086-73_1086-72del MANE Select	NP_000173.2:n.1086-73_1086-72del