Canonical Allele Identifier: CA2727327925
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs2136948018

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120736906_120736908del , CM000674.2:g.120736906_120736908del GRCh38
NC_000012.11:g.121174709_121174711del , CM000674.1:g.121174709_121174711del GRCh37
NC_000012.10:g.119659092_119659094del NCBI36
NG_007991.1:g.16139_16141del

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.211-80_211-78del MANE Select ENSP00000242592.4:n.211-80_211-78del
ENST00000242592.8:c.211-80_211-78del ENSP00000242592.4:n.211-80_211-78del
ENST00000411593.2:c.211-80_211-78del ENSP00000401045.2:n.211-80_211-78del
ENST00000539690.1:n.323-80_323-78del
NM_000017.3:c.211-80_211-78del NP_000008.1:n.211-80_211-78del
NM_001302554.1:c.211-80_211-78del NP_001289483.1:n.211-80_211-78del
NM_000017.4:c.211-80_211-78del MANE Select NP_000008.1:n.211-80_211-78del
NM_001302554.2:c.211-80_211-78del NP_001289483.1:n.211-80_211-78del