Canonical Allele Identifier: CA2841210399
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120727005C>A , CM000674.2:g.120727005C>A GRCh38
NC_000012.11:g.121164808C>A , CM000674.1:g.121164808C>A GRCh37
NC_000012.10:g.119649191C>A NCBI36
NG_007991.1:g.6238C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.47-21C>A MANE Select ENSP00000242592.4:n.47-21C>A
ENST00000242592.8:c.47-21C>A ENSP00000242592.4:n.47-21C>A
ENST00000411593.2:c.47-21C>A ENSP00000401045.2:n.47-21C>A
ENST00000539690.1:n.159-21C>A
NM_000017.3:c.47-21C>A NP_000008.1:n.47-21C>A
NM_001302554.1:c.47-21C>A NP_001289483.1:n.47-21C>A
NM_000017.4:c.47-21C>A MANE Select NP_000008.1:n.47-21C>A
NM_001302554.2:c.47-21C>A NP_001289483.1:n.47-21C>A