Canonical Allele Identifier: CA684418435
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs1310196035

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738765del , CM000674.2:g.120738765del GRCh38
NC_000012.11:g.121176568del , CM000674.1:g.121176568del GRCh37
NC_000012.10:g.119660951del NCBI36
NG_007991.1:g.17998del

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.934-55del MANE Select ENSP00000242592.4:n.934-55del
ENST00000242592.8:c.934-55del ENSP00000242592.4:n.934-55del
ENST00000411593.2:c.922-55del ENSP00000401045.2:n.922-55del
NM_000017.3:c.934-55del NP_000008.1:n.934-55del
NM_001302554.1:c.922-55del NP_001289483.1:n.922-55del
NM_000017.4:c.934-55del MANE Select NP_000008.1:n.934-55del
NM_001302554.2:c.922-55del NP_001289483.1:n.922-55del