Canonical Allele Identifier: CA1167798456

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609382_54609441delinsATAGTCGCCCCCAGCTGGGTTGTGCTCCACTGTGACGGTGGCCCGGGGGGAGGATGCCAG , CM000663.2:g.54609382_54609441delinsATAGTCGCCCCCAGCTGGGTTGTGCTCCACTGTGACGGTGGCCCGGGGGGAGGATGCCAG	GRCh38
NC_000001.10:g.55075055_55075114delinsATAGTCGCCCCCAGCTGGGTTGTGCTCCACTGTGACGGTGGCCCGGGGGGAGGATGCCAG , CM000663.1:g.55075055_55075114delinsATAGTCGCCCCCAGCTGGGTTGTGCTCCACTGTGACGGTGGCCCGGGGGGAGGATGCCAG	GRCh37
NC_000001.9:g.54847643_54847702delinsATAGTCGCCCCCAGCTGGGTTGTGCTCCACTGTGACGGTGGCCCGGGGGGAGGATGCCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1585_1644delinsCTGGCATCCTCCCCCCGGGCCACCGTCACAGTGGAGCACAACCCAGCTGGGGGCGACTAT (FAM151A) MANE Select	ENSP00000306888.2:p.Leu529=
ENST00000343744.7:c.*270_*329delinsATAGTCGCCCCCAGCTGGGTTGTGCTCCACTGTGACGGTGGCCCGGGGGGAGGATGCCAG (ACOT11) MANE Select	ENSP00000340260.2:n.*270_*329delinsATAGTCGCCCCCAGCTGGGTTGTGCT...
ENST00000302250.6:c.1585_1644delinsCTGGCATCCTCCCCCCGGGCCACCGTCACAGTGGAGCACAACCCAGCTGGGGGCGACTAT (FAM151A)	ENSP00000306888.2:p.Leu529=
ENST00000343744.6:c.*270_*329delinsATAGTCGCCCCCAGCTGGGTTGTGCTCCACTGTGACGGTGGCCCGGGGGGAGGATGCCAG (ACOT11)	ENSP00000340260.2:n.*270_*329delinsATAGTCGCCCCCAGCTGGGTTGTGCT...
ENST00000371304.2:c.1024_1083delinsCTGGCATCCTCCCCCCGGGCCACCGTCACAGTGGAGCACAACCCAGCTGGGGGCGACTAT (FAM151A)	ENSP00000360353.2:p.Leu342=
ENST00000371316.3:c.1629+1314_1629+1373delinsATAGTCGCCCCCAGCTGGGTTGTGCTCCACTGTGACGGTGGCCCGGGGGGAGGATGCCAG (ACOT11)	ENSP00000360366.3:n.1629+1314_1629+1373delinsATAGTCGCCCCCAGCT...
ENST00000481208.5:n.2133_2192delinsATAGTCGCCCCCAGCTGGGTTGTGCTCCACTGTGACGGTGGCCCGGGGGGAGGATGCCAG (ACOT11)
NM_015547.3:c.1629+1314_1629+1373delinsATAGTCGCCCCCAGCTGGGTTGTGCTCCACTGTGACGGTGGCCCGGGGGGAGGATGCCAG (ACOT11)	NP_056362.1:n.1629+1314_1629+1373delinsATAGTCGCCCCCAGCTGGGTTG...
NM_147161.3:c.*270_*329delinsATAGTCGCCCCCAGCTGGGTTGTGCTCCACTGTGACGGTGGCCCGGGGGGAGGATGCCAG (ACOT11)	NP_671517.1:n.*270_*329delinsATAGTCGCCCCCAGCTGGGTTGTGCTCCACTG...
NM_176782.2:c.1585_1644delinsCTGGCATCCTCCCCCCGGGCCACCGTCACAGTGGAGCACAACCCAGCTGGGGGCGACTAT (FAM151A)	NP_788954.2:p.Leu529=
XM_006710599.2:c.1507_1566delinsCTGGCATCCTCCCCCCGGGCCACCGTCACAGTGGAGCACAACCCAGCTGGGGGCGACTAT (FAM151A)	XP_006710662.1:p.Leu503=
XM_006710599.3:c.1507_1566delinsCTGGCATCCTCCCCCCGGGCCACCGTCACAGTGGAGCACAACCCAGCTGGGGGCGACTAT (FAM151A)	XP_006710662.1:p.Leu503=
NM_176782.3:c.1585_1644delinsCTGGCATCCTCCCCCCGGGCCACCGTCACAGTGGAGCACAACCCAGCTGGGGGCGACTAT (FAM151A) MANE Select	NP_788954.2:p.Leu529=
NM_015547.4:c.1629+1314_1629+1373delinsATAGTCGCCCCCAGCTGGGTTGTGCTCCACTGTGACGGTGGCCCGGGGGGAGGATGCCAG (ACOT11)	NP_056362.1:n.1629+1314_1629+1373delinsATAGTCGCCCCCAGCTGGGTTG...
NM_147161.4:c.*270_*329delinsATAGTCGCCCCCAGCTGGGTTGTGCTCCACTGTGACGGTGGCCCGGGGGGAGGATGCCAG (ACOT11) MANE Select	NP_671517.1:n.*270_*329delinsATAGTCGCCCCCAGCTGGGTTGTGCTCCACTG...