Canonical Allele Identifier: CA355677881

Gene: EHHADH

Linked Data

• MyVariant Identifiers: chr3:g.184971737C>A (hg19) ; chr3:g.185253949C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185253949C>A , CM000665.2:g.185253949C>A	GRCh38
NC_000003.11:g.184971737C>A , CM000665.1:g.184971737C>A	GRCh37
NC_000003.10:g.186454431C>A	NCBI36
NG_015999.1:g.5150G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231887.8:c.74G>T MANE Select	ENSP00000231887.3:p.Ser25Ile
ENST00000231887.7:c.74G>T	ENSP00000231887.3:p.Ser25Ile
ENST00000440662.1:c.74G>T	ENSP00000396798.1:p.Ser25Ile
ENST00000456310.5:c.-338G>T	ENSP00000387746.1:n.-338G>T
ENST00000465178.1:n.228-5432G>T
ENST00000475987.1:n.101G>T
NM_001166415.1:c.-338G>T	NP_001159887.1:n.-338G>T
NM_001966.3:c.74G>T	NP_001957.2:p.Ser25Ile
XM_006713525.1:c.-582G>T	XP_006713588.1:n.-582G>T
XM_011512517.1:c.-214-5432G>T	XP_011510819.1:n.-214-5432G>T
NM_001966.4:c.74G>T MANE Select	NP_001957.2:p.Ser25Ile
NM_001166415.2:c.-338G>T	NP_001159887.1:n.-338G>T