Canonical Allele Identifier: CA386601684
Gene: ACADS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739168C>A , CM000674.2:g.120739168C>A GRCh38
NC_000012.11:g.121176971C>A , CM000674.1:g.121176971C>A GRCh37
NC_000012.10:g.119661354C>A NCBI36
NG_007991.1:g.18401C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.1058C>A MANE Select ENSP00000242592.4:p.Ser353Ter
ENST00000242592.8:c.1058C>A ENSP00000242592.4:p.Ser353Ter
ENST00000411593.2:c.1046C>A ENSP00000401045.2:p.Ser349Ter
NM_000017.3:c.1058C>A NP_000008.1:p.Ser353Ter
NM_001302554.1:c.1046C>A NP_001289483.1:p.Ser349Ter
NM_000017.4:c.1058C>A MANE Select NP_000008.1:p.Ser353Ter
NM_001302554.2:c.1046C>A NP_001289483.1:p.Ser349Ter