Canonical Allele Identifier: CA1426396517

Gene: EHHADH

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185253927T= , CM000665.2:g.185253927T=	GRCh38
NC_000003.11:g.184971715T= , CM000665.1:g.184971715T=	GRCh37
NC_000003.10:g.186454409T=	NCBI36
NG_015999.1:g.5172A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231887.8:c.74+22A= MANE Select	ENSP00000231887.3:n.74+22A=
ENST00000231887.7:c.74+22A=	ENSP00000231887.3:n.74+22A=
ENST00000440662.1:c.74+22A=	ENSP00000396798.1:n.74+22A=
ENST00000456310.5:c.-316A=	ENSP00000387746.1:n.-316A=
ENST00000465178.1:n.228-5410A=
ENST00000475987.1:n.101+22A=
NM_001166415.1:c.-316A=	NP_001159887.1:n.-316A=
NM_001966.3:c.74+22A=	NP_001957.2:n.74+22A=
XM_006713525.1:c.-582+22A=	XP_006713588.1:n.-582+22A=
XM_011512517.1:c.-214-5410A=	XP_011510819.1:n.-214-5410A=
NM_001966.4:c.74+22A= MANE Select	NP_001957.2:n.74+22A=
NM_001166415.2:c.-316A=	NP_001159887.1:n.-316A=