Canonical Allele Identifier: CA355677930

Gene: EHHADH

Linked Data

• MyVariant Identifiers: chr3:g.184971749A>T (hg19) ; chr3:g.185253961A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185253961A>T , CM000665.2:g.185253961A>T	GRCh38
NC_000003.11:g.184971749A>T , CM000665.1:g.184971749A>T	GRCh37
NC_000003.10:g.186454443A>T	NCBI36
NG_015999.1:g.5138T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231887.8:c.62T>A MANE Select	ENSP00000231887.3:p.Val21Asp
ENST00000231887.7:c.62T>A	ENSP00000231887.3:p.Val21Asp
ENST00000440662.1:c.62T>A	ENSP00000396798.1:p.Val21Asp
ENST00000456310.5:c.-350T>A	ENSP00000387746.1:n.-350T>A
ENST00000465178.1:n.228-5444T>A
ENST00000475987.1:n.89T>A
NM_001166415.1:c.-350T>A	NP_001159887.1:n.-350T>A
NM_001966.3:c.62T>A	NP_001957.2:p.Val21Asp
XM_006713525.1:c.-594T>A	XP_006713588.1:n.-594T>A
XM_011512517.1:c.-214-5444T>A	XP_011510819.1:n.-214-5444T>A
NM_001966.4:c.62T>A MANE Select	NP_001957.2:p.Val21Asp
NM_001166415.2:c.-350T>A	NP_001159887.1:n.-350T>A