Canonical Allele Identifier: CA1167798528

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609536_54609553delinsATATCTGTGAGCAGCTGT , CM000663.2:g.54609536_54609553delinsATATCTGTGAGCAGCTGT	GRCh38
NC_000001.10:g.55075209_55075226delinsATATCTGTGAGCAGCTGT , CM000663.1:g.55075209_55075226delinsATATCTGTGAGCAGCTGT	GRCh37
NC_000001.9:g.54847797_54847814delinsATATCTGTGAGCAGCTGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1473_1490delinsACAGCTGCTCACAGATAT (FAM151A) MANE Select	ENSP00000306888.2:p.Glu491=
ENST00000343744.7:c.*424_*441delinsATATCTGTGAGCAGCTGT (ACOT11) MANE Select	ENSP00000340260.2:n.*424_*441delinsATATCTGTGAGCAGCTGT
ENST00000302250.6:c.1473_1490delinsACAGCTGCTCACAGATAT (FAM151A)	ENSP00000306888.2:p.Glu491=
ENST00000343744.6:c.*424_*441delinsATATCTGTGAGCAGCTGT (ACOT11)	ENSP00000340260.2:n.*424_*441delinsATATCTGTGAGCAGCTGT
ENST00000371304.2:c.918-6_929delinsACAGCTGCTCACAGATAT (FAM151A)
ENST00000371316.3:c.1629+1468_1629+1485delinsATATCTGTGAGCAGCTGT (ACOT11)	ENSP00000360366.3:n.1629+1468_1629+1485delinsATATCTGTGAGCAGCT...
ENST00000481208.5:n.2287_2304delinsATATCTGTGAGCAGCTGT (ACOT11)
NM_015547.3:c.1629+1468_1629+1485delinsATATCTGTGAGCAGCTGT (ACOT11)	NP_056362.1:n.1629+1468_1629+1485delinsATATCTGTGAGCAGCTGT
NM_147161.3:c.*424_*441delinsATATCTGTGAGCAGCTGT (ACOT11)	NP_671517.1:n.*424_*441delinsATATCTGTGAGCAGCTGT
NM_176782.2:c.1473_1490delinsACAGCTGCTCACAGATAT (FAM151A)	NP_788954.2:p.Glu491=
XM_006710599.2:c.1395_1412delinsACAGCTGCTCACAGATAT (FAM151A)	XP_006710662.1:p.Glu465=
XM_006710599.3:c.1395_1412delinsACAGCTGCTCACAGATAT (FAM151A)	XP_006710662.1:p.Glu465=
NM_176782.3:c.1473_1490delinsACAGCTGCTCACAGATAT (FAM151A) MANE Select	NP_788954.2:p.Glu491=
NM_015547.4:c.1629+1468_1629+1485delinsATATCTGTGAGCAGCTGT (ACOT11)	NP_056362.1:n.1629+1468_1629+1485delinsATATCTGTGAGCAGCTGT
NM_147161.4:c.*424_*441delinsATATCTGTGAGCAGCTGT (ACOT11) MANE Select	NP_671517.1:n.*424_*441delinsATATCTGTGAGCAGCTGT