Canonical Allele Identifier: CA2621365356
Gene: ACADS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120736847G>A , CM000674.2:g.120736847G>A GRCh38
NC_000012.11:g.121174650G>A , CM000674.1:g.121174650G>A GRCh37
NC_000012.10:g.119659033G>A NCBI36
NG_007991.1:g.16080G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.211-139G>A MANE Select ENSP00000242592.4:n.211-139G>A
ENST00000242592.8:c.211-139G>A ENSP00000242592.4:n.211-139G>A
ENST00000411593.2:c.211-139G>A ENSP00000401045.2:n.211-139G>A
ENST00000539690.1:n.323-139G>A
NM_000017.3:c.211-139G>A NP_000008.1:n.211-139G>A
NM_001302554.1:c.211-139G>A NP_001289483.1:n.211-139G>A
NM_000017.4:c.211-139G>A MANE Select NP_000008.1:n.211-139G>A
NM_001302554.2:c.211-139G>A NP_001289483.1:n.211-139G>A