Canonical Allele Identifier: CA2067555635
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs1592941227

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739010T>G , CM000674.2:g.120739010T>G GRCh38
NC_000012.11:g.121176813T>G , CM000674.1:g.121176813T>G GRCh37
NC_000012.10:g.119661196T>G NCBI36
NG_007991.1:g.18243T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.1029+95T>G MANE Select ENSP00000242592.4:n.1029+95T>G
ENST00000242592.8:c.1029+95T>G ENSP00000242592.4:n.1029+95T>G
ENST00000411593.2:c.1017+95T>G ENSP00000401045.2:n.1017+95T>G
NM_000017.3:c.1029+95T>G NP_000008.1:n.1029+95T>G
NM_001302554.1:c.1017+95T>G NP_001289483.1:n.1017+95T>G
NM_000017.4:c.1029+95T>G MANE Select NP_000008.1:n.1029+95T>G
NM_001302554.2:c.1017+95T>G NP_001289483.1:n.1017+95T>G