Canonical Allele Identifier: CA1167798547

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609569_54609585delinsCCCAGCACCTCCTCAGG , CM000663.2:g.54609569_54609585delinsCCCAGCACCTCCTCAGG	GRCh38
NC_000001.10:g.55075242_55075258delinsCCCAGCACCTCCTCAGG , CM000663.1:g.55075242_55075258delinsCCCAGCACCTCCTCAGG	GRCh37
NC_000001.9:g.54847830_54847846delinsCCCAGCACCTCCTCAGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1441_1457delinsCCTGAGGAGGTGCTGGG (FAM151A) MANE Select	ENSP00000306888.2:p.Pro481=
ENST00000343744.7:c.*457_*473delinsCCCAGCACCTCCTCAGG (ACOT11) MANE Select	ENSP00000340260.2:n.*457_*473delinsCCCAGCACCTCCTCAGG
ENST00000302250.6:c.1441_1457delinsCCTGAGGAGGTGCTGGG (FAM151A)	ENSP00000306888.2:p.Pro481=
ENST00000343744.6:c.*457_*473delinsCCCAGCACCTCCTCAGG (ACOT11)	ENSP00000340260.2:n.*457_*473delinsCCCAGCACCTCCTCAGG
ENST00000371304.2:c.918-38_918-22delinsCCTGAGGAGGTGCTGGG (FAM151A)	ENSP00000360353.2:n.918-38_918-22delinsCCTGAGGAGGTGCTGGG
ENST00000371316.3:c.1629+1501_1629+1517delinsCCCAGCACCTCCTCAGG (ACOT11)	ENSP00000360366.3:n.1629+1501_1629+1517delinsCCCAGCACCTCCTCAG...
ENST00000481208.5:n.2320_2336delinsCCCAGCACCTCCTCAGG (ACOT11)
NM_015547.3:c.1629+1501_1629+1517delinsCCCAGCACCTCCTCAGG (ACOT11)	NP_056362.1:n.1629+1501_1629+1517delinsCCCAGCACCTCCTCAGG
NM_147161.3:c.*457_*473delinsCCCAGCACCTCCTCAGG (ACOT11)	NP_671517.1:n.*457_*473delinsCCCAGCACCTCCTCAGG
NM_176782.2:c.1441_1457delinsCCTGAGGAGGTGCTGGG (FAM151A)	NP_788954.2:p.Pro481=
XM_006710599.2:c.1363_1379delinsCCTGAGGAGGTGCTGGG (FAM151A)	XP_006710662.1:p.Pro455=
XM_006710599.3:c.1363_1379delinsCCTGAGGAGGTGCTGGG (FAM151A)	XP_006710662.1:p.Pro455=
NM_176782.3:c.1441_1457delinsCCTGAGGAGGTGCTGGG (FAM151A) MANE Select	NP_788954.2:p.Pro481=
NM_015547.4:c.1629+1501_1629+1517delinsCCCAGCACCTCCTCAGG (ACOT11)	NP_056362.1:n.1629+1501_1629+1517delinsCCCAGCACCTCCTCAGG
NM_147161.4:c.*457_*473delinsCCCAGCACCTCCTCAGG (ACOT11) MANE Select	NP_671517.1:n.*457_*473delinsCCCAGCACCTCCTCAGG