Canonical Allele Identifier: CA2743674404

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609673dup , CM000663.2:g.54609673dup	GRCh38
NC_000001.10:g.55075346dup , CM000663.1:g.55075346dup	GRCh37
NC_000001.9:g.54847934dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1357dup (FAM151A) MANE Select	ENSP00000306888.2:p.Ser453PhefsTer17
ENST00000343744.7:c.*561dup (ACOT11) MANE Select	ENSP00000340260.2:n.*561dup
ENST00000302250.6:c.1357dup (FAM151A)	ENSP00000306888.2:p.Ser453PhefsTer17
ENST00000343744.6:c.*561dup (ACOT11)	ENSP00000340260.2:n.*561dup
ENST00000371304.2:c.918-122dup (FAM151A)	ENSP00000360353.2:n.918-122dup
ENST00000371316.3:c.1629+1605dup (ACOT11)	ENSP00000360366.3:n.1629+1605dup
ENST00000481208.5:n.2424dup (ACOT11)
NM_015547.3:c.1629+1605dup (ACOT11)	NP_056362.1:n.1629+1605dup
NM_147161.3:c.*561dup (ACOT11)	NP_671517.1:n.*561dup
NM_176782.2:c.1357dup (FAM151A)	NP_788954.2:p.Ser453PhefsTer17
XM_006710599.2:c.1279dup (FAM151A)	XP_006710662.1:p.Ser427PhefsTer17
XM_006710599.3:c.1279dup (FAM151A)	XP_006710662.1:p.Ser427PhefsTer17
NM_176782.3:c.1357dup (FAM151A) MANE Select	NP_788954.2:p.Ser453PhefsTer17
NM_015547.4:c.1629+1605dup (ACOT11)	NP_056362.1:n.1629+1605dup
NM_147161.4:c.*561dup (ACOT11) MANE Select	NP_671517.1:n.*561dup