Canonical Allele Identifier: CA866829

Gene: FAM151A ACOT11

Linked Data

• dbSNP Id: rs767004485
• ExAC: 1:55074961 C / T
• gnomAD v2: 1-55074961-C-T
• gnomAD v3: 1-54609288-C-T
• gnomAD v4: 1-54609288-C-T
• MyVariant Identifiers: chr1:g.55074961C>T (hg19) ; chr1:g.54609288C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609288C>T , CM000663.2:g.54609288C>T	GRCh38
NC_000001.10:g.55074961C>T , CM000663.1:g.55074961C>T	GRCh37
NC_000001.9:g.54847549C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1738G>A (FAM151A) MANE Select	ENSP00000306888.2:p.Ala580Thr
ENST00000343744.7:c.*176C>T (ACOT11) MANE Select	ENSP00000340260.2:n.*176C>T
ENST00000302250.6:c.1738G>A (FAM151A)	ENSP00000306888.2:p.Ala580Thr
ENST00000343744.6:c.*176C>T (ACOT11)	ENSP00000340260.2:n.*176C>T
ENST00000371304.2:c.1177G>A (FAM151A)	ENSP00000360353.2:p.Ala393Thr
ENST00000371316.3:c.1629+1220C>T (ACOT11)	ENSP00000360366.3:n.1629+1220C>T
ENST00000481208.5:n.2039C>T (ACOT11)
NM_015547.3:c.1629+1220C>T (ACOT11)	NP_056362.1:n.1629+1220C>T
NM_147161.3:c.*176C>T (ACOT11)	NP_671517.1:n.*176C>T
NM_176782.2:c.1738G>A (FAM151A)	NP_788954.2:p.Ala580Thr
XM_006710599.2:c.1660G>A (FAM151A)	XP_006710662.1:p.Ala554Thr
XM_006710599.3:c.1660G>A (FAM151A)	XP_006710662.1:p.Ala554Thr
NM_176782.3:c.1738G>A (FAM151A) MANE Select	NP_788954.2:p.Ala580Thr
NM_015547.4:c.1629+1220C>T (ACOT11)	NP_056362.1:n.1629+1220C>T
NM_147161.4:c.*176C>T (ACOT11) MANE Select	NP_671517.1:n.*176C>T