Canonical Allele Identifier: CA1167798430

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609314_54609324delinsGGTAGCCTGTA , CM000663.2:g.54609314_54609324delinsGGTAGCCTGTA	GRCh38
NC_000001.10:g.55074987_55074997delinsGGTAGCCTGTA , CM000663.1:g.55074987_55074997delinsGGTAGCCTGTA	GRCh37
NC_000001.9:g.54847575_54847585delinsGGTAGCCTGTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1702_1712delinsTACAGGCTACC (FAM151A) MANE Select	ENSP00000306888.2:p.Tyr568=
ENST00000343744.7:c.*202_*212delinsGGTAGCCTGTA (ACOT11) MANE Select	ENSP00000340260.2:n.*202_*212delinsGGTAGCCTGTA
ENST00000302250.6:c.1702_1712delinsTACAGGCTACC (FAM151A)	ENSP00000306888.2:p.Tyr568=
ENST00000343744.6:c.*202_*212delinsGGTAGCCTGTA (ACOT11)	ENSP00000340260.2:n.*202_*212delinsGGTAGCCTGTA
ENST00000371304.2:c.1141_1151delinsTACAGGCTACC (FAM151A)	ENSP00000360353.2:p.Tyr381=
ENST00000371316.3:c.1629+1246_1629+1256delinsGGTAGCCTGTA (ACOT11)	ENSP00000360366.3:n.1629+1246_1629+1256delinsGGTAGCCTGTA
ENST00000481208.5:n.2065_2075delinsGGTAGCCTGTA (ACOT11)
NM_015547.3:c.1629+1246_1629+1256delinsGGTAGCCTGTA (ACOT11)	NP_056362.1:n.1629+1246_1629+1256delinsGGTAGCCTGTA
NM_147161.3:c.*202_*212delinsGGTAGCCTGTA (ACOT11)	NP_671517.1:n.*202_*212delinsGGTAGCCTGTA
NM_176782.2:c.1702_1712delinsTACAGGCTACC (FAM151A)	NP_788954.2:p.Tyr568=
XM_006710599.2:c.1624_1634delinsTACAGGCTACC (FAM151A)	XP_006710662.1:p.Tyr542=
XM_006710599.3:c.1624_1634delinsTACAGGCTACC (FAM151A)	XP_006710662.1:p.Tyr542=
NM_176782.3:c.1702_1712delinsTACAGGCTACC (FAM151A) MANE Select	NP_788954.2:p.Tyr568=
NM_015547.4:c.1629+1246_1629+1256delinsGGTAGCCTGTA (ACOT11)	NP_056362.1:n.1629+1246_1629+1256delinsGGTAGCCTGTA
NM_147161.4:c.*202_*212delinsGGTAGCCTGTA (ACOT11) MANE Select	NP_671517.1:n.*202_*212delinsGGTAGCCTGTA