Canonical Allele Identifier: CA2067555957
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739558A= , CM000674.2:g.120739558A= GRCh38
NC_000012.11:g.121177361A= , CM000674.1:g.121177361A= GRCh37
NC_000012.10:g.119661744A= NCBI36
NG_007991.1:g.18791A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.*110A= MANE Select ENSP00000242592.4:n.*110A=
ENST00000242592.8:c.*110A= ENSP00000242592.4:n.*110A=
ENST00000411593.2:c.*110A= ENSP00000401045.2:n.*110A=
NM_000017.3:c.*110A= NP_000008.1:n.*110A=
NM_001302554.1:c.*110A= NP_001289483.1:n.*110A=
NM_000017.4:c.*110A= MANE Select NP_000008.1:n.*110A=
NM_001302554.2:c.*110A= NP_001289483.1:n.*110A=