Canonical Allele Identifier: CA1167798611

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609710C= , CM000663.2:g.54609710C=	GRCh38
NC_000001.10:g.55075383C= , CM000663.1:g.55075383C=	GRCh37
NC_000001.9:g.54847971C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1316G= (FAM151A) MANE Select	ENSP00000306888.2:p.Trp439=
ENST00000343744.7:c.*598C= (ACOT11) MANE Select	ENSP00000340260.2:n.*598C=
ENST00000302250.6:c.1316G= (FAM151A)	ENSP00000306888.2:p.Trp439=
ENST00000343744.6:c.*598C= (ACOT11)	ENSP00000340260.2:n.*598C=
ENST00000371304.2:c.918-163G= (FAM151A)	ENSP00000360353.2:n.918-163G=
ENST00000371316.3:c.1629+1642C= (ACOT11)	ENSP00000360366.3:n.1629+1642C=
ENST00000481208.5:n.2461C= (ACOT11)
NM_015547.3:c.1629+1642C= (ACOT11)	NP_056362.1:n.1629+1642C=
NM_147161.3:c.*598C= (ACOT11)	NP_671517.1:n.*598C=
NM_176782.2:c.1316G= (FAM151A)	NP_788954.2:p.Trp439=
XM_006710599.2:c.1238G= (FAM151A)	XP_006710662.1:p.Trp413=
XM_006710599.3:c.1238G= (FAM151A)	XP_006710662.1:p.Trp413=
NM_176782.3:c.1316G= (FAM151A) MANE Select	NP_788954.2:p.Trp439=
NM_015547.4:c.1629+1642C= (ACOT11)	NP_056362.1:n.1629+1642C=
NM_147161.4:c.*598C= (ACOT11) MANE Select	NP_671517.1:n.*598C=