Canonical Allele Identifier: CA2067555803
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739318T= , CM000674.2:g.120739318T= GRCh38
NC_000012.11:g.121177121T= , CM000674.1:g.121177121T= GRCh37
NC_000012.10:g.119661504T= NCBI36
NG_007991.1:g.18551T=

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.1109T= MANE Select ENSP00000242592.4:p.Met370=
ENST00000242592.8:c.1109T= ENSP00000242592.4:p.Met370=
ENST00000411593.2:c.1097T= ENSP00000401045.2:p.Met366=
NM_000017.3:c.1109T= NP_000008.1:p.Met370=
NM_001302554.1:c.1097T= NP_001289483.1:p.Met366=
NM_000017.4:c.1109T= MANE Select NP_000008.1:p.Met370=
NM_001302554.2:c.1097T= NP_001289483.1:p.Met366=