Canonical Allele Identifier: CA418177299

Gene: FAM151A ACOT11

Linked Data

• MyVariant Identifiers: chr1:g.55075070T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609397T>A , CM000663.2:g.54609397T>A	GRCh38
NC_000001.10:g.55075070T>A , CM000663.1:g.55075070T>A	GRCh37
NC_000001.9:g.54847658T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000302250.7:c.1629A>T (FAM151A) MANE Select	ENSP00000306888.2:p.Pro543=
ENST00000343744.7:c.*285T>A (ACOT11) MANE Select	ENSP00000340260.2:n.*285T>A
ENST00000302250.6:c.1629A>T (FAM151A)	ENSP00000306888.2:p.Pro543=
ENST00000343744.6:c.*285T>A (ACOT11)	ENSP00000340260.2:n.*285T>A
ENST00000371304.2:c.1068A>T (FAM151A)	ENSP00000360353.2:p.Pro356=
ENST00000371316.3:c.1629+1329T>A (ACOT11)	ENSP00000360366.3:n.1629+1329T>A
ENST00000481208.5:n.2148T>A (ACOT11)
NM_015547.3:c.1629+1329T>A (ACOT11)	NP_056362.1:n.1629+1329T>A
NM_147161.3:c.*285T>A (ACOT11)	NP_671517.1:n.*285T>A
NM_176782.2:c.1629A>T (FAM151A)	NP_788954.2:p.Pro543=
XM_006710599.2:c.1551A>T (FAM151A)	XP_006710662.1:p.Pro517=
XM_006710599.3:c.1551A>T (FAM151A)	XP_006710662.1:p.Pro517=
NM_176782.3:c.1629A>T (FAM151A) MANE Select	NP_788954.2:p.Pro543=
NM_015547.4:c.1629+1329T>A (ACOT11)	NP_056362.1:n.1629+1329T>A
NM_147161.4:c.*285T>A (ACOT11) MANE Select	NP_671517.1:n.*285T>A