Canonical Allele Identifier: CA2621369018
Gene: ACADS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738766C>G , CM000674.2:g.120738766C>G GRCh38
NC_000012.11:g.121176569C>G , CM000674.1:g.121176569C>G GRCh37
NC_000012.10:g.119660952C>G NCBI36
NG_007991.1:g.17999C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.934-54C>G MANE Select ENSP00000242592.4:n.934-54C>G
ENST00000242592.8:c.934-54C>G ENSP00000242592.4:n.934-54C>G
ENST00000411593.2:c.922-54C>G ENSP00000401045.2:n.922-54C>G
NM_000017.3:c.934-54C>G NP_000008.1:n.934-54C>G
NM_001302554.1:c.922-54C>G NP_001289483.1:n.922-54C>G
NM_000017.4:c.934-54C>G MANE Select NP_000008.1:n.934-54C>G
NM_001302554.2:c.922-54C>G NP_001289483.1:n.922-54C>G