Canonical Allele Identifier: CA2067553053
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs1883458067

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120736896A>G , CM000674.2:g.120736896A>G GRCh38
NC_000012.11:g.121174699A>G , CM000674.1:g.121174699A>G GRCh37
NC_000012.10:g.119659082A>G NCBI36
NG_007991.1:g.16129A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.211-90A>G MANE Select ENSP00000242592.4:n.211-90A>G
ENST00000242592.8:c.211-90A>G ENSP00000242592.4:n.211-90A>G
ENST00000411593.2:c.211-90A>G ENSP00000401045.2:n.211-90A>G
ENST00000539690.1:n.323-90A>G
NM_000017.3:c.211-90A>G NP_000008.1:n.211-90A>G
NM_001302554.1:c.211-90A>G NP_001289483.1:n.211-90A>G
NM_000017.4:c.211-90A>G MANE Select NP_000008.1:n.211-90A>G
NM_001302554.2:c.211-90A>G NP_001289483.1:n.211-90A>G