Canonical Allele Identifier: CA2743674401

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609393dup , CM000663.2:g.54609393dup	GRCh38
NC_000001.10:g.55075066dup , CM000663.1:g.55075066dup	GRCh37
NC_000001.9:g.54847654dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1637dup (FAM151A) MANE Select	ENSP00000306888.2:p.Asp547ArgfsTer13
ENST00000343744.7:c.*281dup (ACOT11) MANE Select	ENSP00000340260.2:n.*281dup
ENST00000302250.6:c.1637dup (FAM151A)	ENSP00000306888.2:p.Asp547ArgfsTer13
ENST00000343744.6:c.*281dup (ACOT11)	ENSP00000340260.2:n.*281dup
ENST00000371304.2:c.1076dup (FAM151A)	ENSP00000360353.2:p.Asp360ArgfsTer13
ENST00000371316.3:c.1629+1325dup (ACOT11)	ENSP00000360366.3:n.1629+1325dup
ENST00000481208.5:n.2144dup (ACOT11)
NM_015547.3:c.1629+1325dup (ACOT11)	NP_056362.1:n.1629+1325dup
NM_147161.3:c.*281dup (ACOT11)	NP_671517.1:n.*281dup
NM_176782.2:c.1637dup (FAM151A)	NP_788954.2:p.Asp547ArgfsTer13
XM_006710599.2:c.1559dup (FAM151A)	XP_006710662.1:p.Asp521ArgfsTer13
XM_006710599.3:c.1559dup (FAM151A)	XP_006710662.1:p.Asp521ArgfsTer13
NM_176782.3:c.1637dup (FAM151A) MANE Select	NP_788954.2:p.Asp547ArgfsTer13
NM_015547.4:c.1629+1325dup (ACOT11)	NP_056362.1:n.1629+1325dup
NM_147161.4:c.*281dup (ACOT11) MANE Select	NP_671517.1:n.*281dup