Canonical Allele Identifier: CA736991888

Gene: ACOT11 FAM151A

Linked Data

• dbSNP Id: rs564547713
• gnomAD v3: 1-54609178-G-C
• gnomAD v4: 1-54609178-G-C
• MyVariant Identifiers: chr1:g.55074851G>C (hg19) ; chr1:g.54609178G>C (hg38)

Genomic Alleles

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

Transcript Alleles

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