Canonical Allele Identifier: CA1426371590

Gene: EHHADH

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185228061C= , CM000665.2:g.185228061C=	GRCh38
NC_000003.11:g.184945849C= , CM000665.1:g.184945849C=	GRCh37
NC_000003.10:g.186428543C=	NCBI36
NG_015999.1:g.31038G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231887.8:c.463+1371G= MANE Select	ENSP00000231887.3:n.463+1371G=
ENST00000231887.7:c.463+1371G=	ENSP00000231887.3:n.463+1371G=
ENST00000456310.5:c.175+1371G=	ENSP00000387746.1:n.175+1371G=
ENST00000475987.1:n.491-1203G=
ENST00000483104.5:n.173+7229G=
NM_001166415.1:c.175+1371G=	NP_001159887.1:n.175+1371G=
NM_001966.3:c.463+1371G=	NP_001957.2:n.463+1371G=
XM_006713525.1:c.-192-1203G=	XP_006713588.1:n.-192-1203G=
XM_011512517.1:c.175+1371G=	XP_011510819.1:n.175+1371G=
NM_001966.4:c.463+1371G= MANE Select	NP_001957.2:n.463+1371G=
NM_001166415.2:c.175+1371G=	NP_001159887.1:n.175+1371G=