Canonical Allele Identifier: CA2067555497
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs1883548095

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738775_120738776dup , CM000674.2:g.120738775_120738776dup GRCh38
NC_000012.11:g.121176578_121176579dup , CM000674.1:g.121176578_121176579dup GRCh37
NC_000012.10:g.119660961_119660962dup NCBI36
NG_007991.1:g.18008_18009dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.934-45_934-44dup MANE Select ENSP00000242592.4:n.934-45_934-44dup
ENST00000242592.8:c.934-45_934-44dup ENSP00000242592.4:n.934-45_934-44dup
ENST00000411593.2:c.922-45_922-44dup ENSP00000401045.2:n.922-45_922-44dup
NM_000017.3:c.934-45_934-44dup NP_000008.1:n.934-45_934-44dup
NM_001302554.1:c.922-45_922-44dup NP_001289483.1:n.922-45_922-44dup
NM_000017.4:c.934-45_934-44dup MANE Select NP_000008.1:n.934-45_934-44dup
NM_001302554.2:c.922-45_922-44dup NP_001289483.1:n.922-45_922-44dup