Canonical Allele Identifier: CA2645794464

Gene: FAM151A ACOT11

Linked Data

• gnomAD v4: 1-54609373-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609374dup , CM000663.2:g.54609374dup	GRCh38
NC_000001.10:g.55075047dup , CM000663.1:g.55075047dup	GRCh37
NC_000001.9:g.54847635dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1652dup (FAM151A) MANE Select	ENSP00000306888.2:p.Arg552GlufsTer8
ENST00000343744.7:c.*262dup (ACOT11) MANE Select	ENSP00000340260.2:n.*262dup
ENST00000302250.6:c.1652dup (FAM151A)	ENSP00000306888.2:p.Arg552GlufsTer8
ENST00000343744.6:c.*262dup (ACOT11)	ENSP00000340260.2:n.*262dup
ENST00000371304.2:c.1091dup (FAM151A)	ENSP00000360353.2:p.Arg365GlufsTer8
ENST00000371316.3:c.1629+1306dup (ACOT11)	ENSP00000360366.3:n.1629+1306dup
ENST00000481208.5:n.2125dup (ACOT11)
NM_015547.3:c.1629+1306dup (ACOT11)	NP_056362.1:n.1629+1306dup
NM_147161.3:c.*262dup (ACOT11)	NP_671517.1:n.*262dup
NM_176782.2:c.1652dup (FAM151A)	NP_788954.2:p.Arg552GlufsTer8
XM_006710599.2:c.1574dup (FAM151A)	XP_006710662.1:p.Arg526GlufsTer8
XM_006710599.3:c.1574dup (FAM151A)	XP_006710662.1:p.Arg526GlufsTer8
NM_176782.3:c.1652dup (FAM151A) MANE Select	NP_788954.2:p.Arg552GlufsTer8
NM_015547.4:c.1629+1306dup (ACOT11)	NP_056362.1:n.1629+1306dup
NM_147161.4:c.*262dup (ACOT11) MANE Select	NP_671517.1:n.*262dup