Canonical Allele Identifier: CA355677961

Gene: EHHADH

Linked Data

• gnomAD v4: 3-185253968-G-C
• MyVariant Identifiers: chr3:g.184971756G>C (hg19) ; chr3:g.185253968G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185253968G>C , CM000665.2:g.185253968G>C	GRCh38
NC_000003.11:g.184971756G>C , CM000665.1:g.184971756G>C	GRCh37
NC_000003.10:g.186454450G>C	NCBI36
NG_015999.1:g.5131C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231887.8:c.55C>G MANE Select	ENSP00000231887.3:p.Pro19Ala
ENST00000231887.7:c.55C>G	ENSP00000231887.3:p.Pro19Ala
ENST00000440662.1:c.55C>G	ENSP00000396798.1:p.Pro19Ala
ENST00000456310.5:c.-357C>G	ENSP00000387746.1:n.-357C>G
ENST00000465178.1:n.228-5451C>G
ENST00000475987.1:n.82C>G
NM_001166415.1:c.-357C>G	NP_001159887.1:n.-357C>G
NM_001966.3:c.55C>G	NP_001957.2:p.Pro19Ala
XM_006713525.1:c.-601C>G	XP_006713588.1:n.-601C>G
XM_011512517.1:c.-214-5451C>G	XP_011510819.1:n.-214-5451C>G
NM_001966.4:c.55C>G MANE Select	NP_001957.2:p.Pro19Ala
NM_001166415.2:c.-357C>G	NP_001159887.1:n.-357C>G