Canonical Allele Identifier: CA2658215442

Gene: HADHA

Linked Data

• gnomAD v4: 2-26204042-A-AAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26204051_26204052dup , CM000664.2:g.26204051_26204052dup	GRCh38
NC_000002.11:g.26426920_26426921dup , CM000664.1:g.26426920_26426921dup	GRCh37
NC_000002.10:g.26280424_26280425dup	NCBI36
NG_007121.1:g.45577_45578dup
NG_007121.2:g.45578_45579dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1220+18_1220+19dup MANE Select	ENSP00000370023.3:n.1220+18_1220+19dup
ENST00000492433.2:c.1220+18_1220+19dup	ENSP00000438039.2:n.1220+18_1220+19dup
ENST00000643057.1:c.*1111+18_*1111+19dup	ENSP00000493761.1:n.*1111+18_*1111+19dup
ENST00000643063.1:c.*266+18_*266+19dup	ENSP00000495353.1:n.*266+18_*266+19dup
ENST00000643233.1:c.*1111+18_*1111+19dup	ENSP00000493880.1:n.*1111+18_*1111+19dup
ENST00000644428.1:c.1220+18_1220+19dup	ENSP00000495560.1:n.1220+18_1220+19dup
ENST00000645274.1:c.1115+18_1115+19dup	ENSP00000493996.1:n.1115+18_1115+19dup
ENST00000646031.1:c.579+18_579+19dup
ENST00000646483.1:c.1086+18_1086+19dup	ENSP00000496185.1:n.1086+18_1086+19dup
ENST00000380649.7:c.1220+18_1220+19dup	ENSP00000370023.3:n.1220+18_1220+19dup
NM_000182.4:c.1220+18_1220+19dup	NP_000173.2:n.1220+18_1220+19dup
NM_000182.5:c.1220+18_1220+19dup MANE Select	NP_000173.2:n.1220+18_1220+19dup