Canonical Allele Identifier: CA2645794401
Gene: ACOT11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54609165_54609179dup , CM000663.2:g.54609165_54609179dup GRCh38
NC_000001.10:g.55074838_55074852dup , CM000663.1:g.55074838_55074852dup GRCh37
NC_000001.9:g.54847426_54847440dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000343744.7:c.*53_*67dup MANE Select ENSP00000340260.2:n.*53_*67dup
ENST00000343744.6:c.*53_*67dup ENSP00000340260.2:n.*53_*67dup
ENST00000371316.3:c.1629+1097_1629+1111dup ENSP00000360366.3:n.1629+1097_1629+1111dup
ENST00000481208.5:n.1916_1930dup
NM_015547.3:c.1629+1097_1629+1111dup NP_056362.1:n.1629+1097_1629+1111dup
NM_147161.3:c.*53_*67dup NP_671517.1:n.*53_*67dup
NM_015547.4:c.1629+1097_1629+1111dup NP_056362.1:n.1629+1097_1629+1111dup
NM_147161.4:c.*53_*67dup MANE Select NP_671517.1:n.*53_*67dup