Canonical Allele Identifier: CA1426396625
Gene: EHHADH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254093C= , CM000665.2:g.185254093C= GRCh38
NC_000003.11:g.184971881C= , CM000665.1:g.184971881C= GRCh37
NC_000003.10:g.186454575C= NCBI36
NG_015999.1:g.5006G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231887.7:c.-71G= ENSP00000231887.3:n.-71G=
ENST00000465178.1:n.228-5576G=
NM_001166415.1:c.-482G= NP_001159887.1:n.-482G=
NM_001966.3:c.-71G= NP_001957.2:n.-71G=
XM_011512517.1:c.-214-5576G= XP_011510819.1:n.-214-5576G=