Canonical Allele Identifier: CA1148236303

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609450_54609468delinsCTATGGCTCCAGCTGTGCT , CM000663.2:g.54609450_54609468delinsCTATGGCTCCAGCTGTGCT	GRCh38
NC_000001.10:g.55075123_55075141delinsCTATGGCTCCAGCTGTGCT , CM000663.1:g.55075123_55075141delinsCTATGGCTCCAGCTGTGCT	GRCh37
NC_000001.9:g.54847711_54847729delinsCTATGGCTCCAGCTGTGCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1558_1576delinsAGCACAGCTGGAGCCATAG (FAM151A) MANE Select	ENSP00000306888.2:p.Ser520=
ENST00000343744.7:c.*338_*356delinsCTATGGCTCCAGCTGTGCT (ACOT11) MANE Select	ENSP00000340260.2:n.*338_*356delinsCTATGGCTCCAGCTGTGCT
ENST00000302250.6:c.1558_1576delinsAGCACAGCTGGAGCCATAG (FAM151A)	ENSP00000306888.2:p.Ser520=
ENST00000343744.6:c.*338_*356delinsCTATGGCTCCAGCTGTGCT (ACOT11)	ENSP00000340260.2:n.*338_*356delinsCTATGGCTCCAGCTGTGCT
ENST00000371304.2:c.997_1015delinsAGCACAGCTGGAGCCATAG (FAM151A)	ENSP00000360353.2:p.Ser333=
ENST00000371316.3:c.1629+1382_1629+1400delinsCTATGGCTCCAGCTGTGCT (ACOT11)	ENSP00000360366.3:n.1629+1382_1629+1400delinsCTATGGCTCCAGCTGT...
ENST00000481208.5:n.2201_2219delinsCTATGGCTCCAGCTGTGCT (ACOT11)
NM_015547.3:c.1629+1382_1629+1400delinsCTATGGCTCCAGCTGTGCT (ACOT11)	NP_056362.1:n.1629+1382_1629+1400delinsCTATGGCTCCAGCTGTGCT
NM_147161.3:c.*338_*356delinsCTATGGCTCCAGCTGTGCT (ACOT11)	NP_671517.1:n.*338_*356delinsCTATGGCTCCAGCTGTGCT
NM_176782.2:c.1558_1576delinsAGCACAGCTGGAGCCATAG (FAM151A)	NP_788954.2:p.Ser520=
XM_006710599.2:c.1480_1498delinsAGCACAGCTGGAGCCATAG (FAM151A)	XP_006710662.1:p.Ser494=
XM_006710599.3:c.1480_1498delinsAGCACAGCTGGAGCCATAG (FAM151A)	XP_006710662.1:p.Ser494=
NM_176782.3:c.1558_1576delinsAGCACAGCTGGAGCCATAG (FAM151A) MANE Select	NP_788954.2:p.Ser520=
NM_015547.4:c.1629+1382_1629+1400delinsCTATGGCTCCAGCTGTGCT (ACOT11)	NP_056362.1:n.1629+1382_1629+1400delinsCTATGGCTCCAGCTGTGCT
NM_147161.4:c.*338_*356delinsCTATGGCTCCAGCTGTGCT (ACOT11) MANE Select	NP_671517.1:n.*338_*356delinsCTATGGCTCCAGCTGTGCT