Canonical Allele Identifier: CA2658205347

Gene: HADHA

Linked Data

• gnomAD v4: 2-26204214-AATGACTTTCGGTAAACTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26204217_26204234del , CM000664.2:g.26204217_26204234del	GRCh38
NC_000002.11:g.26427086_26427103del , CM000664.1:g.26427086_26427103del	GRCh37
NC_000002.10:g.26280590_26280607del	NCBI36
NG_007121.1:g.45389_45406del
NG_007121.2:g.45390_45407del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1086-36_1086-19del MANE Select	ENSP00000370023.3:n.1086-36_1086-19del
ENST00000492433.2:c.1086-36_1086-19del	ENSP00000438039.2:n.1086-36_1086-19del
ENST00000643057.1:c.*977-36_*977-19del	ENSP00000493761.1:n.*977-36_*977-19del
ENST00000643063.1:c.*132-36_*132-19del	ENSP00000495353.1:n.*132-36_*132-19del
ENST00000643233.1:c.*977-36_*977-19del	ENSP00000493880.1:n.*977-36_*977-19del
ENST00000644428.1:c.1086-36_1086-19del	ENSP00000495560.1:n.1086-36_1086-19del
ENST00000645274.1:c.981-36_981-19del	ENSP00000493996.1:n.981-36_981-19del
ENST00000646031.1:c.445-36_445-19del
ENST00000646483.1:c.952-36_952-19del	ENSP00000496185.1:n.952-36_952-19del
ENST00000380649.7:c.1086-36_1086-19del	ENSP00000370023.3:n.1086-36_1086-19del
NM_000182.4:c.1086-36_1086-19del	NP_000173.2:n.1086-36_1086-19del
NM_000182.5:c.1086-36_1086-19del MANE Select	NP_000173.2:n.1086-36_1086-19del