Canonical Allele Identifier: CA482146830

Gene: ACADS

Linked Data

• MyVariant Identifiers: chr12:g.121176467C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120738664C>G , CM000674.2:g.120738664C>G	GRCh38
NC_000012.11:g.121176467C>G , CM000674.1:g.121176467C>G	GRCh37
NC_000012.10:g.119660850C>G	NCBI36
NG_007991.1:g.17897C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242592.9:c.927C>G MANE Select	ENSP00000242592.4:p.Val309=
ENST00000242592.8:c.927C>G	ENSP00000242592.4:p.Val309=
ENST00000411593.2:c.915C>G	ENSP00000401045.2:p.Val305=
NM_000017.3:c.927C>G	NP_000008.1:p.Val309=
NM_001302554.1:c.915C>G	NP_001289483.1:p.Val305=
NM_000017.4:c.927C>G MANE Select	NP_000008.1:p.Val309=
NM_001302554.2:c.915C>G	NP_001289483.1:p.Val305=