Canonical Allele Identifier: CA1147076039
Gene: ACOT11 HGNC NCBI
FAM151A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54609178G= , CM000663.2:g.54609178G= GRCh38
NC_000001.10:g.55074851G= , CM000663.1:g.55074851G= GRCh37
NC_000001.9:g.54847439G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000343744.7:c.*66G= (ACOT11) MANE Select ENSP00000340260.2:n.*66G=
ENST00000343744.6:c.*66G= (ACOT11) ENSP00000340260.2:n.*66G=
ENST00000371316.3:c.1629+1110G= (ACOT11) ENSP00000360366.3:n.1629+1110G=
ENST00000481208.5:n.1929G= (ACOT11)
NM_015547.3:c.1629+1110G= (ACOT11) NP_056362.1:n.1629+1110G=
NM_147161.3:c.*66G= (ACOT11) NP_671517.1:n.*66G=
NM_176782.2:c.*90C= (FAM151A) NP_788954.2:n.*90C=
NM_015547.4:c.1629+1110G= (ACOT11) NP_056362.1:n.1629+1110G=
NM_147161.4:c.*66G= (ACOT11) MANE Select NP_671517.1:n.*66G=
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