Canonical Allele Identifier: CA2067555950
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739545C= , CM000674.2:g.120739545C= GRCh38
NC_000012.11:g.121177348C= , CM000674.1:g.121177348C= GRCh37
NC_000012.10:g.119661731C= NCBI36
NG_007991.1:g.18778C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.*97C= MANE Select ENSP00000242592.4:n.*97C=
ENST00000242592.8:c.*97C= ENSP00000242592.4:n.*97C=
ENST00000411593.2:c.*97C= ENSP00000401045.2:n.*97C=
NM_000017.3:c.*97C= NP_000008.1:n.*97C=
NM_001302554.1:c.*97C= NP_001289483.1:n.*97C=
NM_000017.4:c.*97C= MANE Select NP_000008.1:n.*97C=
NM_001302554.2:c.*97C= NP_001289483.1:n.*97C=