Canonical Allele Identifier: CA2067555628
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739004C= , CM000674.2:g.120739004C= GRCh38
NC_000012.11:g.121176807C= , CM000674.1:g.121176807C= GRCh37
NC_000012.10:g.119661190C= NCBI36
NG_007991.1:g.18237C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.1029+89C= MANE Select ENSP00000242592.4:n.1029+89C=
ENST00000242592.8:c.1029+89C= ENSP00000242592.4:n.1029+89C=
ENST00000411593.2:c.1017+89C= ENSP00000401045.2:n.1017+89C=
NM_000017.3:c.1029+89C= NP_000008.1:n.1029+89C=
NM_001302554.1:c.1017+89C= NP_001289483.1:n.1017+89C=
NM_000017.4:c.1029+89C= MANE Select NP_000008.1:n.1029+89C=
NM_001302554.2:c.1017+89C= NP_001289483.1:n.1017+89C=