Canonical Allele Identifier: CA1167798610

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609709C= , CM000663.2:g.54609709C=	GRCh38
NC_000001.10:g.55075382C= , CM000663.1:g.55075382C=	GRCh37
NC_000001.9:g.54847970C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1317G= (FAM151A) MANE Select	ENSP00000306888.2:p.Trp439=
ENST00000343744.7:c.*597C= (ACOT11) MANE Select	ENSP00000340260.2:n.*597C=
ENST00000302250.6:c.1317G= (FAM151A)	ENSP00000306888.2:p.Trp439=
ENST00000343744.6:c.*597C= (ACOT11)	ENSP00000340260.2:n.*597C=
ENST00000371304.2:c.918-162G= (FAM151A)	ENSP00000360353.2:n.918-162G=
ENST00000371316.3:c.1629+1641C= (ACOT11)	ENSP00000360366.3:n.1629+1641C=
ENST00000481208.5:n.2460C= (ACOT11)
NM_015547.3:c.1629+1641C= (ACOT11)	NP_056362.1:n.1629+1641C=
NM_147161.3:c.*597C= (ACOT11)	NP_671517.1:n.*597C=
NM_176782.2:c.1317G= (FAM151A)	NP_788954.2:p.Trp439=
XM_006710599.2:c.1239G= (FAM151A)	XP_006710662.1:p.Trp413=
XM_006710599.3:c.1239G= (FAM151A)	XP_006710662.1:p.Trp413=
NM_176782.3:c.1317G= (FAM151A) MANE Select	NP_788954.2:p.Trp439=
NM_015547.4:c.1629+1641C= (ACOT11)	NP_056362.1:n.1629+1641C=
NM_147161.4:c.*597C= (ACOT11) MANE Select	NP_671517.1:n.*597C=