Canonical Allele Identifier: CA2645794405
Gene: ACOT11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54609171_54609190del , CM000663.2:g.54609171_54609190del GRCh38
NC_000001.10:g.55074844_55074863del , CM000663.1:g.55074844_55074863del GRCh37
NC_000001.9:g.54847432_54847451del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000343744.7:c.*59_*78del MANE Select ENSP00000340260.2:n.*59_*78del
ENST00000343744.6:c.*59_*78del ENSP00000340260.2:n.*59_*78del
ENST00000371316.3:c.1629+1103_1629+1122del ENSP00000360366.3:n.1629+1103_1629+1122del
ENST00000481208.5:n.1922_1941del
NM_015547.3:c.1629+1103_1629+1122del NP_056362.1:n.1629+1103_1629+1122del
NM_147161.3:c.*59_*78del NP_671517.1:n.*59_*78del
NM_015547.4:c.1629+1103_1629+1122del NP_056362.1:n.1629+1103_1629+1122del
NM_147161.4:c.*59_*78del MANE Select NP_671517.1:n.*59_*78del