Canonical Allele Identifier: CA2645794467

Gene: FAM151A ACOT11

Linked Data

• gnomAD v4: 1-54609395-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609396dup , CM000663.2:g.54609396dup	GRCh38
NC_000001.10:g.55075069dup , CM000663.1:g.55075069dup	GRCh37
NC_000001.9:g.54847657dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000302250.7:c.1630dup (FAM151A) MANE Select	ENSP00000306888.2:p.Ala544GlyfsTer16
ENST00000343744.7:c.*284dup (ACOT11) MANE Select	ENSP00000340260.2:n.*284dup
ENST00000302250.6:c.1630dup (FAM151A)	ENSP00000306888.2:p.Ala544GlyfsTer16
ENST00000343744.6:c.*284dup (ACOT11)	ENSP00000340260.2:n.*284dup
ENST00000371304.2:c.1069dup (FAM151A)	ENSP00000360353.2:p.Ala357GlyfsTer16
ENST00000371316.3:c.1629+1328dup (ACOT11)	ENSP00000360366.3:n.1629+1328dup
ENST00000481208.5:n.2147dup (ACOT11)
NM_015547.3:c.1629+1328dup (ACOT11)	NP_056362.1:n.1629+1328dup
NM_147161.3:c.*284dup (ACOT11)	NP_671517.1:n.*284dup
NM_176782.2:c.1630dup (FAM151A)	NP_788954.2:p.Ala544GlyfsTer16
XM_006710599.2:c.1552dup (FAM151A)	XP_006710662.1:p.Ala518GlyfsTer16
XM_006710599.3:c.1552dup (FAM151A)	XP_006710662.1:p.Ala518GlyfsTer16
NM_176782.3:c.1630dup (FAM151A) MANE Select	NP_788954.2:p.Ala544GlyfsTer16
NM_015547.4:c.1629+1328dup (ACOT11)	NP_056362.1:n.1629+1328dup
NM_147161.4:c.*284dup (ACOT11) MANE Select	NP_671517.1:n.*284dup