Canonical Allele Identifier: CA1149132472

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609590C= , CM000663.2:g.54609590C=	GRCh38
NC_000001.10:g.55075263C= , CM000663.1:g.55075263C=	GRCh37
NC_000001.9:g.54847851C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1436G= (FAM151A) MANE Select	ENSP00000306888.2:p.Gly479=
ENST00000343744.7:c.*478C= (ACOT11) MANE Select	ENSP00000340260.2:n.*478C=
ENST00000302250.6:c.1436G= (FAM151A)	ENSP00000306888.2:p.Gly479=
ENST00000343744.6:c.*478C= (ACOT11)	ENSP00000340260.2:n.*478C=
ENST00000371304.2:c.918-43G= (FAM151A)	ENSP00000360353.2:n.918-43G=
ENST00000371316.3:c.1629+1522C= (ACOT11)	ENSP00000360366.3:n.1629+1522C=
ENST00000481208.5:n.2341C= (ACOT11)
NM_015547.3:c.1629+1522C= (ACOT11)	NP_056362.1:n.1629+1522C=
NM_147161.3:c.*478C= (ACOT11)	NP_671517.1:n.*478C=
NM_176782.2:c.1436G= (FAM151A)	NP_788954.2:p.Gly479=
XM_006710599.2:c.1358G= (FAM151A)	XP_006710662.1:p.Gly453=
XM_006710599.3:c.1358G= (FAM151A)	XP_006710662.1:p.Gly453=
NM_176782.3:c.1436G= (FAM151A) MANE Select	NP_788954.2:p.Gly479=
NM_015547.4:c.1629+1522C= (ACOT11)	NP_056362.1:n.1629+1522C=
NM_147161.4:c.*478C= (ACOT11) MANE Select	NP_671517.1:n.*478C=