Canonical Allele Identifier: CA2067555554
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738868A= , CM000674.2:g.120738868A= GRCh38
NC_000012.11:g.121176671A= , CM000674.1:g.121176671A= GRCh37
NC_000012.10:g.119661054A= NCBI36
NG_007991.1:g.18101A=

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.982A= MANE Select ENSP00000242592.4:p.Thr328=
ENST00000242592.8:c.982A= ENSP00000242592.4:p.Thr328=
ENST00000411593.2:c.970A= ENSP00000401045.2:p.Thr324=
NM_000017.3:c.982A= NP_000008.1:p.Thr328=
NM_001302554.1:c.970A= NP_001289483.1:p.Thr324=
NM_000017.4:c.982A= MANE Select NP_000008.1:p.Thr328=
NM_001302554.2:c.970A= NP_001289483.1:p.Thr324=