Canonical Allele Identifier: CA22715199

Gene: ACOT11 FAM151A

Linked Data

• dbSNP Id: rs954417786
• COSMIC: COSN8474269
• MyVariant Identifiers: chr1:g.55074850T>G (hg19) ; chr1:g.54609177T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609177T>G , CM000663.2:g.54609177T>G	GRCh38
NC_000001.10:g.55074850T>G , CM000663.1:g.55074850T>G	GRCh37
NC_000001.9:g.54847438T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343744.7:c.*65T>G (ACOT11) MANE Select	ENSP00000340260.2:n.*65T>G
ENST00000343744.6:c.*65T>G (ACOT11)	ENSP00000340260.2:n.*65T>G
ENST00000371316.3:c.1629+1109T>G (ACOT11)	ENSP00000360366.3:n.1629+1109T>G
ENST00000481208.5:n.1928T>G (ACOT11)
NM_015547.3:c.1629+1109T>G (ACOT11)	NP_056362.1:n.1629+1109T>G
NM_147161.3:c.*65T>G (ACOT11)	NP_671517.1:n.*65T>G
NM_176782.2:c.*91A>C (FAM151A)	NP_788954.2:n.*91A>C
NM_015547.4:c.1629+1109T>G (ACOT11)	NP_056362.1:n.1629+1109T>G
NM_147161.4:c.*65T>G (ACOT11) MANE Select	NP_671517.1:n.*65T>G