Canonical Allele Identifier: CA1167798589

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609646G= , CM000663.2:g.54609646G=	GRCh38
NC_000001.10:g.55075319G= , CM000663.1:g.55075319G=	GRCh37
NC_000001.9:g.54847907G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1380C= (FAM151A) MANE Select	ENSP00000306888.2:p.Gly460=
ENST00000343744.7:c.*534G= (ACOT11) MANE Select	ENSP00000340260.2:n.*534G=
ENST00000302250.6:c.1380C= (FAM151A)	ENSP00000306888.2:p.Gly460=
ENST00000343744.6:c.*534G= (ACOT11)	ENSP00000340260.2:n.*534G=
ENST00000371304.2:c.918-99C= (FAM151A)	ENSP00000360353.2:n.918-99C=
ENST00000371316.3:c.1629+1578G= (ACOT11)	ENSP00000360366.3:n.1629+1578G=
ENST00000481208.5:n.2397G= (ACOT11)
NM_015547.3:c.1629+1578G= (ACOT11)	NP_056362.1:n.1629+1578G=
NM_147161.3:c.*534G= (ACOT11)	NP_671517.1:n.*534G=
NM_176782.2:c.1380C= (FAM151A)	NP_788954.2:p.Gly460=
XM_006710599.2:c.1302C= (FAM151A)	XP_006710662.1:p.Gly434=
XM_006710599.3:c.1302C= (FAM151A)	XP_006710662.1:p.Gly434=
NM_176782.3:c.1380C= (FAM151A) MANE Select	NP_788954.2:p.Gly460=
NM_015547.4:c.1629+1578G= (ACOT11)	NP_056362.1:n.1629+1578G=
NM_147161.4:c.*534G= (ACOT11) MANE Select	NP_671517.1:n.*534G=