Canonical Allele Identifier: CA482146802

Gene: ACADS

Linked Data

• gnomAD v4: 12-120738643-G-T
• MyVariant Identifiers: chr12:g.121176446G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120738643G>T , CM000674.2:g.120738643G>T	GRCh38
NC_000012.11:g.121176446G>T , CM000674.1:g.121176446G>T	GRCh37
NC_000012.10:g.119660829G>T	NCBI36
NG_007991.1:g.17876G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242592.9:c.906G>T MANE Select	ENSP00000242592.4:p.Ala302=
ENST00000242592.8:c.906G>T	ENSP00000242592.4:p.Ala302=
ENST00000411593.2:c.894G>T	ENSP00000401045.2:p.Ala298=
NM_000017.3:c.906G>T	NP_000008.1:p.Ala302=
NM_001302554.1:c.894G>T	NP_001289483.1:p.Ala298=
NM_000017.4:c.906G>T MANE Select	NP_000008.1:p.Ala302=
NM_001302554.2:c.894G>T	NP_001289483.1:p.Ala298=