Canonical Allele Identifier: CA2743674406

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609702dup , CM000663.2:g.54609702dup	GRCh38
NC_000001.10:g.55075375dup , CM000663.1:g.55075375dup	GRCh37
NC_000001.9:g.54847963dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1324dup (FAM151A) MANE Select	ENSP00000306888.2:p.Trp442LeufsTer28
ENST00000343744.7:c.*590dup (ACOT11) MANE Select	ENSP00000340260.2:n.*590dup
ENST00000302250.6:c.1324dup (FAM151A)	ENSP00000306888.2:p.Trp442LeufsTer28
ENST00000343744.6:c.*590dup (ACOT11)	ENSP00000340260.2:n.*590dup
ENST00000371304.2:c.918-155dup (FAM151A)	ENSP00000360353.2:n.918-155dup
ENST00000371316.3:c.1629+1634dup (ACOT11)	ENSP00000360366.3:n.1629+1634dup
ENST00000481208.5:n.2453dup (ACOT11)
NM_015547.3:c.1629+1634dup (ACOT11)	NP_056362.1:n.1629+1634dup
NM_147161.3:c.*590dup (ACOT11)	NP_671517.1:n.*590dup
NM_176782.2:c.1324dup (FAM151A)	NP_788954.2:p.Trp442LeufsTer28
XM_006710599.2:c.1246dup (FAM151A)	XP_006710662.1:p.Trp416LeufsTer28
XM_006710599.3:c.1246dup (FAM151A)	XP_006710662.1:p.Trp416LeufsTer28
NM_176782.3:c.1324dup (FAM151A) MANE Select	NP_788954.2:p.Trp442LeufsTer28
NM_015547.4:c.1629+1634dup (ACOT11)	NP_056362.1:n.1629+1634dup
NM_147161.4:c.*590dup (ACOT11) MANE Select	NP_671517.1:n.*590dup