Canonical Allele Identifier: CA355677919

Gene: EHHADH

Linked Data

• MyVariant Identifiers: chr3:g.184971746T>G (hg19) ; chr3:g.185253958T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185253958T>G , CM000665.2:g.185253958T>G	GRCh38
NC_000003.11:g.184971746T>G , CM000665.1:g.184971746T>G	GRCh37
NC_000003.10:g.186454440T>G	NCBI36
NG_015999.1:g.5141A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231887.8:c.65A>C MANE Select	ENSP00000231887.3:p.Asn22Thr
ENST00000231887.7:c.65A>C	ENSP00000231887.3:p.Asn22Thr
ENST00000440662.1:c.65A>C	ENSP00000396798.1:p.Asn22Thr
ENST00000456310.5:c.-347A>C	ENSP00000387746.1:n.-347A>C
ENST00000465178.1:n.228-5441A>C
ENST00000475987.1:n.92A>C
NM_001166415.1:c.-347A>C	NP_001159887.1:n.-347A>C
NM_001966.3:c.65A>C	NP_001957.2:p.Asn22Thr
XM_006713525.1:c.-591A>C	XP_006713588.1:n.-591A>C
XM_011512517.1:c.-214-5441A>C	XP_011510819.1:n.-214-5441A>C
NM_001966.4:c.65A>C MANE Select	NP_001957.2:p.Asn22Thr
NM_001166415.2:c.-347A>C	NP_001159887.1:n.-347A>C