Canonical Allele Identifier: CA2067555802
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739317A= , CM000674.2:g.120739317A= GRCh38
NC_000012.11:g.121177120A= , CM000674.1:g.121177120A= GRCh37
NC_000012.10:g.119661503A= NCBI36
NG_007991.1:g.18550A=

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.1108A= MANE Select ENSP00000242592.4:p.Met370=
ENST00000242592.8:c.1108A= ENSP00000242592.4:p.Met370=
ENST00000411593.2:c.1096A= ENSP00000401045.2:p.Met366=
NM_000017.3:c.1108A= NP_000008.1:p.Met370=
NM_001302554.1:c.1096A= NP_001289483.1:p.Met366=
NM_000017.4:c.1108A= MANE Select NP_000008.1:p.Met370=
NM_001302554.2:c.1096A= NP_001289483.1:p.Met366=