Canonical Allele Identifier: CA1167798557

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609594G= , CM000663.2:g.54609594G=	GRCh38
NC_000001.10:g.55075267G= , CM000663.1:g.55075267G=	GRCh37
NC_000001.9:g.54847855G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1432C= (FAM151A) MANE Select	ENSP00000306888.2:p.Pro478=
ENST00000343744.7:c.*482G= (ACOT11) MANE Select	ENSP00000340260.2:n.*482G=
ENST00000302250.6:c.1432C= (FAM151A)	ENSP00000306888.2:p.Pro478=
ENST00000343744.6:c.*482G= (ACOT11)	ENSP00000340260.2:n.*482G=
ENST00000371304.2:c.918-47C= (FAM151A)	ENSP00000360353.2:n.918-47C=
ENST00000371316.3:c.1629+1526G= (ACOT11)	ENSP00000360366.3:n.1629+1526G=
ENST00000481208.5:n.2345G= (ACOT11)
NM_015547.3:c.1629+1526G= (ACOT11)	NP_056362.1:n.1629+1526G=
NM_147161.3:c.*482G= (ACOT11)	NP_671517.1:n.*482G=
NM_176782.2:c.1432C= (FAM151A)	NP_788954.2:p.Pro478=
XM_006710599.2:c.1354C= (FAM151A)	XP_006710662.1:p.Pro452=
XM_006710599.3:c.1354C= (FAM151A)	XP_006710662.1:p.Pro452=
NM_176782.3:c.1432C= (FAM151A) MANE Select	NP_788954.2:p.Pro478=
NM_015547.4:c.1629+1526G= (ACOT11)	NP_056362.1:n.1629+1526G=
NM_147161.4:c.*482G= (ACOT11) MANE Select	NP_671517.1:n.*482G=