Canonical Allele Identifier: CA2645794413

Gene: ACOT11 FAM151A

Linked Data

• gnomAD v4: 1-54609178-GCCTGGAGAAAGCCAAAGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609182_54609199del , CM000663.2:g.54609182_54609199del	GRCh38
NC_000001.10:g.55074855_55074872del , CM000663.1:g.55074855_55074872del	GRCh37
NC_000001.9:g.54847443_54847460del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343744.7:c.*70_*87del (ACOT11) MANE Select	ENSP00000340260.2:n.*70_*87del
ENST00000343744.6:c.*70_*87del (ACOT11)	ENSP00000340260.2:n.*70_*87del
ENST00000371316.3:c.1629+1114_1629+1131del (ACOT11)	ENSP00000360366.3:n.1629+1114_1629+1131del
ENST00000481208.5:n.1933_1950del (ACOT11)
NM_015547.3:c.1629+1114_1629+1131del (ACOT11)	NP_056362.1:n.1629+1114_1629+1131del
NM_147161.3:c.*70_*87del (ACOT11)	NP_671517.1:n.*70_*87del
NM_176782.2:c.*72_*89del (FAM151A)	NP_788954.2:n.*72_*89del
NM_015547.4:c.1629+1114_1629+1131del (ACOT11)	NP_056362.1:n.1629+1114_1629+1131del
NM_147161.4:c.*70_*87del (ACOT11) MANE Select	NP_671517.1:n.*70_*87del