Canonical Allele Identifier: CA482146800

Gene: ACADS

Linked Data

• MyVariant Identifiers: chr12:g.121176443G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120738640G>T , CM000674.2:g.120738640G>T	GRCh38
NC_000012.11:g.121176443G>T , CM000674.1:g.121176443G>T	GRCh37
NC_000012.10:g.119660826G>T	NCBI36
NG_007991.1:g.17873G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242592.9:c.903G>T MANE Select	ENSP00000242592.4:p.Gly301=
ENST00000242592.8:c.903G>T	ENSP00000242592.4:p.Gly301=
ENST00000411593.2:c.891G>T	ENSP00000401045.2:p.Gly297=
NM_000017.3:c.903G>T	NP_000008.1:p.Gly301=
NM_001302554.1:c.891G>T	NP_001289483.1:p.Gly297=
NM_000017.4:c.903G>T MANE Select	NP_000008.1:p.Gly301=
NM_001302554.2:c.891G>T	NP_001289483.1:p.Gly297=