Canonical Allele Identifier: CA2658215360
Gene: HADHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26203931_26203933del , CM000664.2:g.26203931_26203933del GRCh38
NC_000002.11:g.26426800_26426802del , CM000664.1:g.26426800_26426802del GRCh37
NC_000002.10:g.26280304_26280306del NCBI36
NG_007121.1:g.45690_45692del
NG_007121.2:g.45691_45693del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380649.8:c.1220+131_1220+133del MANE Select ENSP00000370023.3:n.1220+131_1220+133del
ENST00000492433.2:c.1220+131_1220+133del ENSP00000438039.2:n.1220+131_1220+133del
ENST00000643057.1:c.*1111+131_*1111+133del ENSP00000493761.1:n.*1111+131_*1111+133del
ENST00000643063.1:c.*266+131_*266+133del ENSP00000495353.1:n.*266+131_*266+133del
ENST00000643233.1:c.*1111+131_*1111+133del ENSP00000493880.1:n.*1111+131_*1111+133del
ENST00000644428.1:c.1220+131_1220+133del ENSP00000495560.1:n.1220+131_1220+133del
ENST00000645274.1:c.1115+131_1115+133del ENSP00000493996.1:n.1115+131_1115+133del
ENST00000646031.1:c.579+131_579+133del
ENST00000646483.1:c.1086+131_1086+133del ENSP00000496185.1:n.1086+131_1086+133del
ENST00000380649.7:c.1220+131_1220+133del ENSP00000370023.3:n.1220+131_1220+133del
NM_000182.4:c.1220+131_1220+133del NP_000173.2:n.1220+131_1220+133del
NM_000182.5:c.1220+131_1220+133del MANE Select NP_000173.2:n.1220+131_1220+133del