Canonical Allele Identifier: CA482146842

Gene: ACADS

Linked Data

• MyVariant Identifiers: chr12:g.121176473G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120738670G>A , CM000674.2:g.120738670G>A	GRCh38
NC_000012.11:g.121176473G>A , CM000674.1:g.121176473G>A	GRCh37
NC_000012.10:g.119660856G>A	NCBI36
NG_007991.1:g.17903G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242592.9:c.933G>A MANE Select	ENSP00000242592.4:p.Gln311=
ENST00000242592.8:c.933G>A	ENSP00000242592.4:p.Gln311=
ENST00000411593.2:c.921G>A	ENSP00000401045.2:p.Gln307=
NM_000017.3:c.933G>A	NP_000008.1:p.Gln311=
NM_001302554.1:c.921G>A	NP_001289483.1:p.Gln307=
NM_000017.4:c.933G>A MANE Select	NP_000008.1:p.Gln311=
NM_001302554.2:c.921G>A	NP_001289483.1:p.Gln307=