Canonical Allele Identifier: CA2067553426
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120737165A= , CM000674.2:g.120737165A= GRCh38
NC_000012.11:g.121174968A= , CM000674.1:g.121174968A= GRCh37
NC_000012.10:g.119659351A= NCBI36
NG_007991.1:g.16398A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.360+30A= MANE Select ENSP00000242592.4:n.360+30A=
ENST00000242592.8:c.360+30A= ENSP00000242592.4:n.360+30A=
ENST00000411593.2:c.360+30A= ENSP00000401045.2:n.360+30A=
ENST00000539690.1:n.502A=
NM_000017.3:c.360+30A= NP_000008.1:n.360+30A=
NM_001302554.1:c.360+30A= NP_001289483.1:n.360+30A=
NM_000017.4:c.360+30A= MANE Select NP_000008.1:n.360+30A=
NM_001302554.2:c.360+30A= NP_001289483.1:n.360+30A=